Titre : Maladies métaboliques et nutritionnelles

Maladies métaboliques et nutritionnelles : Questions médicales fréquentes

Nom anglais: Nutritional and Metabolic Diseases

Descriptor UI: D009750

Tree Number: C18

Questions fréquentes et termes MeSH associés

Diagnostic 5

#1

Comment diagnostiquer le diabète de type 2 ?

Le diagnostic se fait par des tests de glycémie à jeun et l'HbA1c.
Diabète Glycémie HbA1c
#2

Quels tests pour l'hyperlipidémie ?

Un profil lipidique sanguin mesure les niveaux de cholestérol et triglycérides.
Hyperlipidémie Cholestérol Triglycérides
#3

Comment détecter une carence en fer ?

Des tests sanguins mesurent la ferritine et l'hémoglobine.
Carence en fer Ferritine Hémoglobine
#4

Quels signes indiquent une maladie de Wilson ?

Des tests de cuivre sérique et une biopsie hépatique confirment la maladie.
Maladie de Wilson Cuivre sérique Biopsie hépatique
#5

Comment évaluer l'obésité ?

L'IMC (indice de masse corporelle) est utilisé pour évaluer l'obésité.
Obésité IMC Indice de masse corporelle

Symptômes 5

#1

Quels sont les symptômes du diabète ?

Les symptômes incluent soif excessive, urination fréquente et fatigue.
Diabète Symptômes Fatigue
#2

Comment se manifeste l'hyperthyroïdie ?

Elle se manifeste par perte de poids, nervosité et palpitations.
Hyperthyroïdie Perte de poids Palpitations
#3

Quels signes d'une carence en vitamine D ?

Les signes incluent fatigue, douleurs osseuses et faiblesse musculaire.
Carence en vitamine D Fatigue Douleurs osseuses
#4

Quels symptômes de l'acidocétose diabétique ?

Les symptômes incluent nausées, vomissements et respiration rapide.
Acidocétose diabétique Nausées Respiration rapide
#5

Comment reconnaître une hypoglycémie ?

Les signes incluent tremblements, sueurs et confusion mentale.
Hypoglycémie Tremblements Confusion mentale

Prévention 5

#1

Comment prévenir le diabète de type 2 ?

Un mode de vie sain avec une alimentation équilibrée et de l'exercice aide.
Diabète de type 2 Prévention Alimentation équilibrée
#2

Quelles mesures pour éviter l'obésité ?

Maintenir un poids santé par l'alimentation et l'activité physique régulière.
Obésité Poids santé Activité physique
#3

Comment prévenir les carences nutritionnelles ?

Une alimentation variée et équilibrée est essentielle pour éviter les carences.
Carences nutritionnelles Alimentation variée Équilibre alimentaire
#4

Quelles stratégies pour éviter l'hyperlipidémie ?

Adopter un régime pauvre en graisses saturées et faire de l'exercice régulièrement.
Hyperlipidémie Régime Exercice
#5

Comment prévenir l'acidocétose diabétique ?

Un bon contrôle de la glycémie et une éducation sur le diabète sont cruciaux.
Acidocétose diabétique Contrôle de la glycémie Éducation sur le diabète

Traitements 5

#1

Quel traitement pour le diabète de type 1 ?

Le traitement principal est l'insulinothérapie pour réguler la glycémie.
Diabète de type 1 Insulinothérapie Glycémie
#2

Comment traiter l'hyperlipidémie ?

Les statines et un régime alimentaire adapté sont souvent prescrits.
Hyperlipidémie Statines Régime alimentaire
#3

Quel est le traitement de l'obésité ?

Le traitement inclut un régime, de l'exercice et parfois des médicaments.
Obésité Régime Médicaments
#4

Comment traiter une carence en fer ?

Des suppléments de fer et des modifications alimentaires sont recommandés.
Carence en fer Suppléments de fer Alimentation
#5

Quel traitement pour l'hyperthyroïdie ?

Les traitements incluent des médicaments antithyroïdiens ou l'iode radioactif.
Hyperthyroïdie Médicaments antithyroïdiens Iode radioactif

Complications 5

#1

Quelles complications du diabète ?

Les complications incluent neuropathie, rétinopathie et maladies cardiovasculaires.
Diabète Neuropathie Rétinopathie
#2

Quels risques liés à l'obésité ?

L'obésité augmente le risque de maladies cardiaques, diabète et hypertension.
Obésité Maladies cardiaques Hypertension
#3

Quelles complications de l'hyperlipidémie ?

Elle peut entraîner des maladies coronariennes et des AVC.
Hyperlipidémie Maladies coronariennes AVC
#4

Quels effets d'une carence en vitamine D ?

Une carence peut causer des troubles osseux et un affaiblissement du système immunitaire.
Carence en vitamine D Troubles osseux Système immunitaire
#5

Quelles complications de l'hyperthyroïdie ?

Les complications incluent l'ostéoporose et les troubles cardiaques.
Hyperthyroïdie Ostéoporose Troubles cardiaques

Facteurs de risque 5

#1

Quels facteurs de risque pour le diabète ?

L'obésité, l'inactivité physique et des antécédents familiaux augmentent le risque.
Diabète Obésité Antécédents familiaux
#2

Quels risques liés à l'alimentation pour l'hyperlipidémie ?

Une alimentation riche en graisses saturées et en sucres augmente le risque.
Hyperlipidémie Alimentation Graisses saturées
#3

Quels facteurs de risque pour l'obésité ?

Les facteurs incluent la génétique, le mode de vie et des troubles hormonaux.
Obésité Génétique Troubles hormonaux
#4

Quels risques de carence en fer ?

Les régimes végétariens stricts et les pertes sanguines augmentent le risque.
Carence en fer Régimes végétariens Pertes sanguines
#5

Quels facteurs de risque pour l'hyperthyroïdie ?

Les antécédents familiaux et certaines maladies auto-immunes augmentent le risque.
Hyperthyroïdie Antécédents familiaux Maladies auto-immunes
{ "@context": "https://schema.org", "@graph": [ { "@type": "MedicalWebPage", "name": "Maladies métaboliques et nutritionnelles : Questions médicales les plus fréquentes", "headline": "Maladies métaboliques et nutritionnelles : Comprendre les symptômes, diagnostics et traitements", "description": "Guide complet et accessible sur les Maladies métaboliques et nutritionnelles : explications, diagnostics, traitements et prévention. Information médicale validée destinée aux patients.", "datePublished": "2024-05-07", "dateModified": "2024-11-03", "inLanguage": "fr", "medicalAudience": [ { "@type": "MedicalAudience", "name": "Grand public", "audienceType": "Patient", "healthCondition": { "@type": "MedicalCondition", "name": "Maladies métaboliques et nutritionnelles" }, "suggestedMinAge": 18, "suggestedGender": "unisex" }, { "@type": "MedicalAudience", "name": "Médecins", "audienceType": "Physician", "geographicArea": { "@type": "AdministrativeArea", "name": "France" } }, { "@type": "MedicalAudience", "name": "Chercheurs", "audienceType": "Researcher", "geographicArea": { "@type": "AdministrativeArea", "name": "International" } } ], "reviewedBy": { "@type": "Person", "name": "Dr Olivier Menir", "jobTitle": "Expert en Médecine", "description": "Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale", "url": "/static/pages/docteur-olivier-menir.html", "alumniOf": { "@type": "EducationalOrganization", "name": "Université Paris Descartes" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladies métaboliques", "alternateName": "Metabolic Diseases", "url": "https://recherchemedicale.com/mesh/D008659", "about": { "@type": "MedicalCondition", "name": "Maladies métaboliques", "code": { "@type": "MedicalCode", "code": "D008659", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Troubles de l'équilibre acidobasique", "alternateName": "Acid-Base Imbalance", "url": "https://recherchemedicale.com/mesh/D000137", "about": { "@type": "MedicalCondition", "name": "Troubles de l'équilibre acidobasique", "code": { "@type": "MedicalCode", "code": "D000137", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Achlorhydrie", "alternateName": "Achlorhydria", "url": "https://recherchemedicale.com/mesh/D000126", "about": { "@type": "MedicalCondition", "name": "Achlorhydrie", "code": { "@type": "MedicalCode", "code": "D000126", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.087" } } }, { "@type": "MedicalWebPage", "name": "Acidose", "alternateName": "Acidosis", "url": "https://recherchemedicale.com/mesh/D000138", "about": { "@type": "MedicalCondition", "name": "Acidose", "code": { "@type": "MedicalCode", "code": "D000138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidose lactique", "alternateName": "Acidosis, Lactic", "url": "https://recherchemedicale.com/mesh/D000140", "about": { "@type": "MedicalCondition", "name": "Acidose lactique", "code": { "@type": "MedicalCode", "code": "D000140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.180" } } }, { "@type": "MedicalWebPage", "name": "Acidose tubulaire rénale", "alternateName": "Acidosis, Renal Tubular", "url": "https://recherchemedicale.com/mesh/D000141", "about": { "@type": "MedicalCondition", "name": "Acidose tubulaire rénale", "code": { "@type": "MedicalCode", "code": "D000141", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.210" } } }, { "@type": "MedicalWebPage", "name": "Acidose respiratoire", "alternateName": "Acidosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000142", "about": { "@type": "MedicalCondition", "name": "Acidose respiratoire", "code": { "@type": "MedicalCode", "code": "D000142", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.310" } } }, { "@type": "MedicalWebPage", "name": "Cétose", "alternateName": "Ketosis", "url": "https://recherchemedicale.com/mesh/D007662", "about": { "@type": "MedicalCondition", "name": "Cétose", "code": { "@type": "MedicalCode", "code": "D007662", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.652" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidose lactique", "alternateName": "Acidosis, Lactic", "url": "https://recherchemedicale.com/mesh/D000140", "about": { "@type": "MedicalCondition", "name": "Acidose lactique", "code": { "@type": "MedicalCode", "code": "D000140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.180" } } }, { "@type": "MedicalWebPage", "name": "Acidose tubulaire rénale", "alternateName": "Acidosis, Renal Tubular", "url": "https://recherchemedicale.com/mesh/D000141", "about": { "@type": "MedicalCondition", "name": "Acidose tubulaire rénale", "code": { "@type": "MedicalCode", "code": "D000141", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.210" } } }, { "@type": "MedicalWebPage", "name": "Acidose respiratoire", "alternateName": "Acidosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000142", "about": { "@type": "MedicalCondition", "name": "Acidose respiratoire", "code": { "@type": "MedicalCode", "code": "D000142", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.310" } } }, { "@type": "MedicalWebPage", "name": "Cétose", "alternateName": "Ketosis", "url": "https://recherchemedicale.com/mesh/D007662", "about": { "@type": "MedicalCondition", "name": "Cétose", "code": { "@type": "MedicalCode", "code": "D007662", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.652" } } }, { "@type": "MedicalWebPage", "name": "Alcalose", "alternateName": "Alkalosis", "url": "https://recherchemedicale.com/mesh/D000471", "about": { "@type": "MedicalCondition", "name": "Alcalose", "code": { "@type": "MedicalCode", "code": "D000471", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Alcalose respiratoire", "alternateName": "Alkalosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000472", "about": { "@type": "MedicalCondition", "name": "Alcalose respiratoire", "code": { "@type": "MedicalCode", "code": "D000472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Alcalose respiratoire", "alternateName": "Alkalosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000472", "about": { "@type": "MedicalCondition", "name": "Alcalose respiratoire", "code": { "@type": "MedicalCode", "code": "D000472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Achlorhydrie", "alternateName": "Achlorhydria", "url": "https://recherchemedicale.com/mesh/D000126", "about": { "@type": "MedicalCondition", "name": "Achlorhydrie", "code": { "@type": "MedicalCode", "code": "D000126", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.087" } } }, { "@type": "MedicalWebPage", "name": "Acidose", "alternateName": "Acidosis", "url": "https://recherchemedicale.com/mesh/D000138", "about": { "@type": "MedicalCondition", "name": "Acidose", "code": { "@type": "MedicalCode", "code": "D000138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidose lactique", "alternateName": "Acidosis, Lactic", "url": "https://recherchemedicale.com/mesh/D000140", "about": { "@type": "MedicalCondition", "name": "Acidose lactique", "code": { "@type": "MedicalCode", "code": "D000140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.180" } } }, { "@type": "MedicalWebPage", "name": "Acidose tubulaire rénale", "alternateName": "Acidosis, Renal Tubular", "url": "https://recherchemedicale.com/mesh/D000141", "about": { "@type": "MedicalCondition", "name": "Acidose tubulaire rénale", "code": { "@type": "MedicalCode", "code": "D000141", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.210" } } }, { "@type": "MedicalWebPage", "name": "Acidose respiratoire", "alternateName": "Acidosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000142", "about": { "@type": "MedicalCondition", "name": "Acidose respiratoire", "code": { "@type": "MedicalCode", "code": "D000142", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.310" } } }, { "@type": "MedicalWebPage", "name": "Cétose", "alternateName": "Ketosis", "url": "https://recherchemedicale.com/mesh/D007662", "about": { "@type": "MedicalCondition", "name": "Cétose", "code": { "@type": "MedicalCode", "code": "D007662", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.652" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidose lactique", "alternateName": "Acidosis, Lactic", "url": "https://recherchemedicale.com/mesh/D000140", "about": { "@type": "MedicalCondition", "name": "Acidose lactique", "code": { "@type": "MedicalCode", "code": "D000140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.180" } } }, { "@type": "MedicalWebPage", "name": "Acidose tubulaire rénale", "alternateName": "Acidosis, Renal Tubular", "url": "https://recherchemedicale.com/mesh/D000141", "about": { "@type": "MedicalCondition", "name": "Acidose tubulaire rénale", "code": { "@type": "MedicalCode", "code": "D000141", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.210" } } }, { "@type": "MedicalWebPage", "name": "Acidose respiratoire", "alternateName": "Acidosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000142", "about": { "@type": "MedicalCondition", "name": "Acidose respiratoire", "code": { "@type": "MedicalCode", "code": "D000142", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.310" } } }, { "@type": "MedicalWebPage", "name": "Cétose", "alternateName": "Ketosis", "url": "https://recherchemedicale.com/mesh/D007662", "about": { "@type": "MedicalCondition", "name": "Cétose", "code": { "@type": "MedicalCode", "code": "D007662", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.176.652" } } }, { "@type": "MedicalWebPage", "name": "Alcalose", "alternateName": "Alkalosis", "url": "https://recherchemedicale.com/mesh/D000471", "about": { "@type": "MedicalCondition", "name": "Alcalose", "code": { "@type": "MedicalCode", "code": "D000471", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Alcalose respiratoire", "alternateName": "Alkalosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000472", "about": { "@type": "MedicalCondition", "name": "Alcalose respiratoire", "code": { "@type": "MedicalCode", "code": "D000472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Alcalose respiratoire", "alternateName": "Alkalosis, Respiratory", "url": "https://recherchemedicale.com/mesh/D000472", "about": { "@type": "MedicalCondition", "name": "Alcalose respiratoire", "code": { "@type": "MedicalCode", "code": "D000472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.076.354.271" } } }, { "@type": "MedicalWebPage", "name": "Maladies osseuses métaboliques", "alternateName": "Bone Diseases, Metabolic", "url": "https://recherchemedicale.com/mesh/D001851", "about": { "@type": "MedicalCondition", "name": "Maladies osseuses métaboliques", "code": { "@type": "MedicalCode", "code": "D001851", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déminéralisation osseuse pathologique", "alternateName": "Bone Demineralization, Pathologic", "url": "https://recherchemedicale.com/mesh/D018488", "about": { "@type": "MedicalCondition", "name": "Déminéralisation osseuse pathologique", "code": { "@type": "MedicalCode", "code": "D018488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.247" } } }, { "@type": "MedicalWebPage", "name": "Ostéoporose", "alternateName": "Osteoporosis", "url": "https://recherchemedicale.com/mesh/D010024", "about": { "@type": "MedicalCondition", "name": "Ostéoporose", "code": { "@type": "MedicalCode", "code": "D010024", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéoporose post-ménopausique", "alternateName": "Osteoporosis, Postmenopausal", "url": "https://recherchemedicale.com/mesh/D015663", "about": { "@type": "MedicalCondition", "name": "Ostéoporose post-ménopausique", "code": { "@type": "MedicalCode", "code": "D015663", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579.610" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéoporose post-ménopausique", "alternateName": "Osteoporosis, Postmenopausal", "url": "https://recherchemedicale.com/mesh/D015663", "about": { "@type": "MedicalCondition", "name": "Ostéoporose post-ménopausique", "code": { "@type": "MedicalCode", "code": "D015663", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579.610" } } } ] }, { "@type": "MedicalWebPage", "name": "Déminéralisation osseuse pathologique", "alternateName": "Bone Demineralization, Pathologic", "url": "https://recherchemedicale.com/mesh/D018488", "about": { "@type": "MedicalCondition", "name": "Déminéralisation osseuse pathologique", "code": { "@type": "MedicalCode", "code": "D018488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.247" } } }, { "@type": "MedicalWebPage", "name": "Ostéoporose", "alternateName": "Osteoporosis", "url": "https://recherchemedicale.com/mesh/D010024", "about": { "@type": "MedicalCondition", "name": "Ostéoporose", "code": { "@type": "MedicalCode", "code": "D010024", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéoporose post-ménopausique", "alternateName": "Osteoporosis, Postmenopausal", "url": "https://recherchemedicale.com/mesh/D015663", "about": { "@type": "MedicalCondition", "name": "Ostéoporose post-ménopausique", "code": { "@type": "MedicalCode", "code": "D015663", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579.610" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéoporose post-ménopausique", "alternateName": "Osteoporosis, Postmenopausal", "url": "https://recherchemedicale.com/mesh/D015663", "about": { "@type": "MedicalCondition", "name": "Ostéoporose post-ménopausique", "code": { "@type": "MedicalCode", "code": "D015663", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.104.579.610" } } }, { "@type": "MedicalWebPage", "name": "Encéphalopathies métaboliques", "alternateName": "Brain Diseases, Metabolic", "url": "https://recherchemedicale.com/mesh/D001928", "about": { "@type": "MedicalCondition", "name": "Encéphalopathies métaboliques", "code": { "@type": "MedicalCode", "code": "D001928", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Encéphalopathie hépatique", "alternateName": "Hepatic Encephalopathy", "url": "https://recherchemedicale.com/mesh/D006501", "about": { "@type": "MedicalCondition", "name": "Encéphalopathie hépatique", "code": { "@type": "MedicalCode", "code": "D006501", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.360" } } }, { "@type": "MedicalWebPage", "name": "Myélinolyse centropontine", "alternateName": "Myelinolysis, Central Pontine", "url": "https://recherchemedicale.com/mesh/D017590", "about": { "@type": "MedicalCondition", "name": "Myélinolyse centropontine", "code": { "@type": "MedicalCode", "code": "D017590", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.560" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Reye", "alternateName": "Reye Syndrome", "url": "https://recherchemedicale.com/mesh/D012202", "about": { "@type": "MedicalCondition", "name": "Syndrome de Reye", "code": { "@type": "MedicalCode", "code": "D012202", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.780" } } } ] }, { "@type": "MedicalWebPage", "name": "Encéphalopathie hépatique", "alternateName": "Hepatic Encephalopathy", "url": "https://recherchemedicale.com/mesh/D006501", "about": { "@type": "MedicalCondition", "name": "Encéphalopathie hépatique", "code": { "@type": "MedicalCode", "code": "D006501", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.360" } } }, { "@type": "MedicalWebPage", "name": "Myélinolyse centropontine", "alternateName": "Myelinolysis, Central Pontine", "url": "https://recherchemedicale.com/mesh/D017590", "about": { "@type": "MedicalCondition", "name": "Myélinolyse centropontine", "code": { "@type": "MedicalCode", "code": "D017590", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.560" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Reye", "alternateName": "Reye Syndrome", "url": "https://recherchemedicale.com/mesh/D012202", "about": { "@type": "MedicalCondition", "name": "Syndrome de Reye", "code": { "@type": "MedicalCode", "code": "D012202", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.132.780" } } }, { "@type": "MedicalWebPage", "name": "Troubles du métabolisme du calcium", "alternateName": "Calcium Metabolism Disorders", "url": "https://recherchemedicale.com/mesh/D002128", "about": { "@type": "MedicalCondition", "name": "Troubles du métabolisme du calcium", "code": { "@type": "MedicalCode", "code": "D002128", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Calcinose", "alternateName": "Calcinosis", "url": "https://recherchemedicale.com/mesh/D002114", "about": { "@type": "MedicalCondition", "name": "Calcinose", "code": { "@type": "MedicalCode", "code": "D002114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Calcinose cutanée", "alternateName": "Calcinosis Cutis", "url": "https://recherchemedicale.com/mesh/D000092182", "about": { "@type": "MedicalCondition", "name": "Calcinose cutanée", "code": { "@type": "MedicalCode", "code": "D000092182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.093" } } }, { "@type": "MedicalWebPage", "name": "Calciphylaxie", "alternateName": "Calciphylaxis", "url": "https://recherchemedicale.com/mesh/D002115", "about": { "@type": "MedicalCondition", "name": "Calciphylaxie", "code": { "@type": "MedicalCode", "code": "D002115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.186" } } }, { "@type": "MedicalWebPage", "name": "Syndrome CREST", "alternateName": "CREST Syndrome", "url": "https://recherchemedicale.com/mesh/D017675", "about": { "@type": "MedicalCondition", "name": "Syndrome CREST", "code": { "@type": "MedicalCode", "code": "D017675", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.204" } } }, { "@type": "MedicalWebPage", "name": "Néphrocalcinose", "alternateName": "Nephrocalcinosis", "url": "https://recherchemedicale.com/mesh/D009397", "about": { "@type": "MedicalCondition", "name": "Néphrocalcinose", "code": { "@type": "MedicalCode", "code": "D009397", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.560" } } }, { "@type": "MedicalWebPage", "name": "Calcification vasculaire", "alternateName": "Vascular Calcification", "url": "https://recherchemedicale.com/mesh/D061205", "about": { "@type": "MedicalCondition", "name": "Calcification vasculaire", "code": { "@type": "MedicalCode", "code": "D061205", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Calcinose cutanée", "alternateName": "Calcinosis Cutis", "url": "https://recherchemedicale.com/mesh/D000092182", "about": { "@type": "MedicalCondition", "name": "Calcinose cutanée", "code": { "@type": "MedicalCode", "code": "D000092182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.093" } } }, { "@type": "MedicalWebPage", "name": "Calciphylaxie", "alternateName": "Calciphylaxis", "url": "https://recherchemedicale.com/mesh/D002115", "about": { "@type": "MedicalCondition", "name": "Calciphylaxie", "code": { "@type": "MedicalCode", "code": "D002115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.186" } } }, { "@type": "MedicalWebPage", "name": "Syndrome CREST", "alternateName": "CREST Syndrome", "url": "https://recherchemedicale.com/mesh/D017675", "about": { "@type": "MedicalCondition", "name": "Syndrome CREST", "code": { "@type": "MedicalCode", "code": "D017675", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.204" } } }, { "@type": "MedicalWebPage", "name": "Néphrocalcinose", "alternateName": "Nephrocalcinosis", "url": "https://recherchemedicale.com/mesh/D009397", "about": { "@type": "MedicalCondition", "name": "Néphrocalcinose", "code": { "@type": "MedicalCode", "code": "D009397", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.560" } } }, { "@type": "MedicalWebPage", "name": "Calcification vasculaire", "alternateName": "Vascular Calcification", "url": "https://recherchemedicale.com/mesh/D061205", "about": { "@type": "MedicalCondition", "name": "Calcification vasculaire", "code": { "@type": "MedicalCode", "code": "D061205", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } }, { "@type": "MedicalWebPage", "name": "Décalcification osseuse", "alternateName": "Decalcification, Pathologic", "url": "https://recherchemedicale.com/mesh/D003649", "about": { "@type": "MedicalCondition", "name": "Décalcification osseuse", "code": { "@type": "MedicalCode", "code": "D003649", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.289" } } } ] }, { "@type": "MedicalWebPage", "name": "Calcinose", "alternateName": "Calcinosis", "url": "https://recherchemedicale.com/mesh/D002114", "about": { "@type": "MedicalCondition", "name": "Calcinose", "code": { "@type": "MedicalCode", "code": "D002114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Calcinose cutanée", "alternateName": "Calcinosis Cutis", "url": "https://recherchemedicale.com/mesh/D000092182", "about": { "@type": "MedicalCondition", "name": "Calcinose cutanée", "code": { "@type": "MedicalCode", "code": "D000092182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.093" } } }, { "@type": "MedicalWebPage", "name": "Calciphylaxie", "alternateName": "Calciphylaxis", "url": "https://recherchemedicale.com/mesh/D002115", "about": { "@type": "MedicalCondition", "name": "Calciphylaxie", "code": { "@type": "MedicalCode", "code": "D002115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.186" } } }, { "@type": "MedicalWebPage", "name": "Syndrome CREST", "alternateName": "CREST Syndrome", "url": "https://recherchemedicale.com/mesh/D017675", "about": { "@type": "MedicalCondition", "name": "Syndrome CREST", "code": { "@type": "MedicalCode", "code": "D017675", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.204" } } }, { "@type": "MedicalWebPage", "name": "Néphrocalcinose", "alternateName": "Nephrocalcinosis", "url": "https://recherchemedicale.com/mesh/D009397", "about": { "@type": "MedicalCondition", "name": "Néphrocalcinose", "code": { "@type": "MedicalCode", "code": "D009397", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.560" } } }, { "@type": "MedicalWebPage", "name": "Calcification vasculaire", "alternateName": "Vascular Calcification", "url": "https://recherchemedicale.com/mesh/D061205", "about": { "@type": "MedicalCondition", "name": "Calcification vasculaire", "code": { "@type": "MedicalCode", "code": "D061205", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Calcinose cutanée", "alternateName": "Calcinosis Cutis", "url": "https://recherchemedicale.com/mesh/D000092182", "about": { "@type": "MedicalCondition", "name": "Calcinose cutanée", "code": { "@type": "MedicalCode", "code": "D000092182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.093" } } }, { "@type": "MedicalWebPage", "name": "Calciphylaxie", "alternateName": "Calciphylaxis", "url": "https://recherchemedicale.com/mesh/D002115", "about": { "@type": "MedicalCondition", "name": "Calciphylaxie", "code": { "@type": "MedicalCode", "code": "D002115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.186" } } }, { "@type": "MedicalWebPage", "name": "Syndrome CREST", "alternateName": "CREST Syndrome", "url": "https://recherchemedicale.com/mesh/D017675", "about": { "@type": "MedicalCondition", "name": "Syndrome CREST", "code": { "@type": "MedicalCode", "code": "D017675", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.204" } } }, { "@type": "MedicalWebPage", "name": "Néphrocalcinose", "alternateName": "Nephrocalcinosis", "url": "https://recherchemedicale.com/mesh/D009397", "about": { "@type": "MedicalCondition", "name": "Néphrocalcinose", "code": { "@type": "MedicalCode", "code": "D009397", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.560" } } }, { "@type": "MedicalWebPage", "name": "Calcification vasculaire", "alternateName": "Vascular Calcification", "url": "https://recherchemedicale.com/mesh/D061205", "about": { "@type": "MedicalCondition", "name": "Calcification vasculaire", "code": { "@type": "MedicalCode", "code": "D061205", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose de Mönckeberg", "alternateName": "Monckeberg Medial Calcific Sclerosis", "url": "https://recherchemedicale.com/mesh/D050380", "about": { "@type": "MedicalCondition", "name": "Sclérose de Mönckeberg", "code": { "@type": "MedicalCode", "code": "D050380", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.130.780.500" } } }, { "@type": "MedicalWebPage", "name": "Décalcification osseuse", "alternateName": "Decalcification, Pathologic", "url": "https://recherchemedicale.com/mesh/D003649", "about": { "@type": "MedicalCondition", "name": "Décalcification osseuse", "code": { "@type": "MedicalCode", "code": "D003649", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.174.289" } } }, { "@type": "MedicalWebPage", "name": "Troubles dus à un défaut de réparation de l'ADN", "alternateName": "DNA Repair-Deficiency Disorders", "url": "https://recherchemedicale.com/mesh/D049914", "about": { "@type": "MedicalCondition", "name": "Troubles dus à un défaut de réparation de l'ADN", "code": { "@type": "MedicalCode", "code": "D049914", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de Cockayne", "alternateName": "Cockayne Syndrome", "url": "https://recherchemedicale.com/mesh/D003057", "about": { "@type": "MedicalCondition", "name": "Syndrome de Cockayne", "code": { "@type": "MedicalCode", "code": "D003057", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.250" } } }, { "@type": "MedicalWebPage", "name": "Tumeurs colorectales héréditaires sans polypose", "alternateName": "Colorectal Neoplasms, Hereditary Nonpolyposis", "url": "https://recherchemedicale.com/mesh/D003123", "about": { "@type": "MedicalCondition", "name": "Tumeurs colorectales héréditaires sans polypose", "code": { "@type": "MedicalCode", "code": "D003123", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.255" } } }, { "@type": "MedicalWebPage", "name": "Anémie de Fanconi", "alternateName": "Fanconi Anemia", "url": "https://recherchemedicale.com/mesh/D005199", "about": { "@type": "MedicalCondition", "name": "Anémie de Fanconi", "code": { "@type": "MedicalCode", "code": "D005199", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.280" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Li-Fraumeni", "alternateName": "Li-Fraumeni Syndrome", "url": "https://recherchemedicale.com/mesh/D016864", "about": { "@type": "MedicalCondition", "name": "Syndrome de Li-Fraumeni", "code": { "@type": "MedicalCode", "code": "D016864", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des cassures de Nijmegen", "alternateName": "Nijmegen Breakage Syndrome", "url": "https://recherchemedicale.com/mesh/D049932", "about": { "@type": "MedicalCondition", "name": "Syndrome des cassures de Nijmegen", "code": { "@type": "MedicalCode", "code": "D049932", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.600" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Rothmund-Thomson", "alternateName": "Rothmund-Thomson Syndrome", "url": "https://recherchemedicale.com/mesh/D011038", "about": { "@type": "MedicalCondition", "name": "Syndrome de Rothmund-Thomson", "code": { "@type": "MedicalCode", "code": "D011038", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.760" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Werner", "alternateName": "Werner Syndrome", "url": "https://recherchemedicale.com/mesh/D014898", "about": { "@type": "MedicalCondition", "name": "Syndrome de Werner", "code": { "@type": "MedicalCode", "code": "D014898", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.960" } } }, { "@type": "MedicalWebPage", "name": "Xeroderma pigmentosum", "alternateName": "Xeroderma Pigmentosum", "url": "https://recherchemedicale.com/mesh/D014983", "about": { "@type": "MedicalCondition", "name": "Xeroderma pigmentosum", "code": { "@type": "MedicalCode", "code": "D014983", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.975" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de Cockayne", "alternateName": "Cockayne Syndrome", "url": "https://recherchemedicale.com/mesh/D003057", "about": { "@type": "MedicalCondition", "name": "Syndrome de Cockayne", "code": { "@type": "MedicalCode", "code": "D003057", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.250" } } }, { "@type": "MedicalWebPage", "name": "Tumeurs colorectales héréditaires sans polypose", "alternateName": "Colorectal Neoplasms, Hereditary Nonpolyposis", "url": "https://recherchemedicale.com/mesh/D003123", "about": { "@type": "MedicalCondition", "name": "Tumeurs colorectales héréditaires sans polypose", "code": { "@type": "MedicalCode", "code": "D003123", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.255" } } }, { "@type": "MedicalWebPage", "name": "Anémie de Fanconi", "alternateName": "Fanconi Anemia", "url": "https://recherchemedicale.com/mesh/D005199", "about": { "@type": "MedicalCondition", "name": "Anémie de Fanconi", "code": { "@type": "MedicalCode", "code": "D005199", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.280" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Li-Fraumeni", "alternateName": "Li-Fraumeni Syndrome", "url": "https://recherchemedicale.com/mesh/D016864", "about": { "@type": "MedicalCondition", "name": "Syndrome de Li-Fraumeni", "code": { "@type": "MedicalCode", "code": "D016864", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des cassures de Nijmegen", "alternateName": "Nijmegen Breakage Syndrome", "url": "https://recherchemedicale.com/mesh/D049932", "about": { "@type": "MedicalCondition", "name": "Syndrome des cassures de Nijmegen", "code": { "@type": "MedicalCode", "code": "D049932", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.600" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Rothmund-Thomson", "alternateName": "Rothmund-Thomson Syndrome", "url": "https://recherchemedicale.com/mesh/D011038", "about": { "@type": "MedicalCondition", "name": "Syndrome de Rothmund-Thomson", "code": { "@type": "MedicalCode", "code": "D011038", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.760" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Werner", "alternateName": "Werner Syndrome", "url": "https://recherchemedicale.com/mesh/D014898", "about": { "@type": "MedicalCondition", "name": "Syndrome de Werner", "code": { "@type": "MedicalCode", "code": "D014898", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.960" } } }, { "@type": "MedicalWebPage", "name": "Xeroderma pigmentosum", "alternateName": "Xeroderma Pigmentosum", "url": "https://recherchemedicale.com/mesh/D014983", "about": { "@type": "MedicalCondition", "name": "Xeroderma pigmentosum", "code": { "@type": "MedicalCode", "code": "D014983", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.284.975" } } }, { "@type": "MedicalWebPage", "name": "Troubles du métabolisme du glucose", "alternateName": "Glucose Metabolism Disorders", "url": "https://recherchemedicale.com/mesh/D044882", "about": { "@type": "MedicalCondition", "name": "Troubles du métabolisme du glucose", "code": { "@type": "MedicalCode", "code": "D044882", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycosurie", "alternateName": "Glycosuria", "url": "https://recherchemedicale.com/mesh/D006029", "about": { "@type": "MedicalCondition", "name": "Glycosurie", "code": { "@type": "MedicalCode", "code": "D006029", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycosurie rénale", "alternateName": "Glycosuria, Renal", "url": "https://recherchemedicale.com/mesh/D006030", "about": { "@type": "MedicalCondition", "name": "Glycosurie rénale", "code": { "@type": "MedicalCode", "code": "D006030", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937.450" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycosurie rénale", "alternateName": "Glycosuria, Renal", "url": "https://recherchemedicale.com/mesh/D006030", "about": { "@type": "MedicalCondition", "name": "Glycosurie rénale", "code": { "@type": "MedicalCode", "code": "D006030", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycémie", "alternateName": "Hyperglycemia", "url": "https://recherchemedicale.com/mesh/D006943", "about": { "@type": "MedicalCondition", "name": "Hyperglycémie", "code": { "@type": "MedicalCode", "code": "D006943", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Intolérance au glucose", "alternateName": "Glucose Intolerance", "url": "https://recherchemedicale.com/mesh/D018149", "about": { "@type": "MedicalCondition", "name": "Intolérance au glucose", "code": { "@type": "MedicalCode", "code": "D018149", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Intolérance au glucose", "alternateName": "Glucose Intolerance", "url": "https://recherchemedicale.com/mesh/D018149", "about": { "@type": "MedicalCondition", "name": "Intolérance au glucose", "code": { "@type": "MedicalCode", "code": "D018149", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperinsulinisme", "alternateName": "Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D006946", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme", "code": { "@type": "MedicalCode", "code": "D006946", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.968" } } }, { "@type": "MedicalWebPage", "name": "Hypoglycémie", "alternateName": "Hypoglycemia", "url": "https://recherchemedicale.com/mesh/D007003", "about": { "@type": "MedicalCondition", "name": "Hypoglycémie", "code": { "@type": "MedicalCode", "code": "D007003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperinsulinisme congénital", "alternateName": "Congenital Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D044903", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme congénital", "code": { "@type": "MedicalCode", "code": "D044903", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } }, { "@type": "MedicalWebPage", "name": "Coma insulinique", "alternateName": "Insulin Coma", "url": "https://recherchemedicale.com/mesh/D007331", "about": { "@type": "MedicalCondition", "name": "Coma insulinique", "code": { "@type": "MedicalCode", "code": "D007331", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.492" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperinsulinisme congénital", "alternateName": "Congenital Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D044903", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme congénital", "code": { "@type": "MedicalCode", "code": "D044903", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } }, { "@type": "MedicalWebPage", "name": "Coma insulinique", "alternateName": "Insulin Coma", "url": "https://recherchemedicale.com/mesh/D007331", "about": { "@type": "MedicalCondition", "name": "Coma insulinique", "code": { "@type": "MedicalCode", "code": "D007331", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.492" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycosurie", "alternateName": "Glycosuria", "url": "https://recherchemedicale.com/mesh/D006029", "about": { "@type": "MedicalCondition", "name": "Glycosurie", "code": { "@type": "MedicalCode", "code": "D006029", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycosurie rénale", "alternateName": "Glycosuria, Renal", "url": "https://recherchemedicale.com/mesh/D006030", "about": { "@type": "MedicalCondition", "name": "Glycosurie rénale", "code": { "@type": "MedicalCode", "code": "D006030", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937.450" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycosurie rénale", "alternateName": "Glycosuria, Renal", "url": "https://recherchemedicale.com/mesh/D006030", "about": { "@type": "MedicalCondition", "name": "Glycosurie rénale", "code": { "@type": "MedicalCode", "code": "D006030", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.937.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycémie", "alternateName": "Hyperglycemia", "url": "https://recherchemedicale.com/mesh/D006943", "about": { "@type": "MedicalCondition", "name": "Hyperglycémie", "code": { "@type": "MedicalCode", "code": "D006943", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Intolérance au glucose", "alternateName": "Glucose Intolerance", "url": "https://recherchemedicale.com/mesh/D018149", "about": { "@type": "MedicalCondition", "name": "Intolérance au glucose", "code": { "@type": "MedicalCode", "code": "D018149", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Intolérance au glucose", "alternateName": "Glucose Intolerance", "url": "https://recherchemedicale.com/mesh/D018149", "about": { "@type": "MedicalCondition", "name": "Intolérance au glucose", "code": { "@type": "MedicalCode", "code": "D018149", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.952.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperinsulinisme", "alternateName": "Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D006946", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme", "code": { "@type": "MedicalCode", "code": "D006946", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.968" } } }, { "@type": "MedicalWebPage", "name": "Hypoglycémie", "alternateName": "Hypoglycemia", "url": "https://recherchemedicale.com/mesh/D007003", "about": { "@type": "MedicalCondition", "name": "Hypoglycémie", "code": { "@type": "MedicalCode", "code": "D007003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperinsulinisme congénital", "alternateName": "Congenital Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D044903", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme congénital", "code": { "@type": "MedicalCode", "code": "D044903", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } }, { "@type": "MedicalWebPage", "name": "Coma insulinique", "alternateName": "Insulin Coma", "url": "https://recherchemedicale.com/mesh/D007331", "about": { "@type": "MedicalCondition", "name": "Coma insulinique", "code": { "@type": "MedicalCode", "code": "D007331", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.492" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperinsulinisme congénital", "alternateName": "Congenital Hyperinsulinism", "url": "https://recherchemedicale.com/mesh/D044903", "about": { "@type": "MedicalCondition", "name": "Hyperinsulinisme congénital", "code": { "@type": "MedicalCode", "code": "D044903", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Nésidioblastose", "alternateName": "Nesidioblastosis", "url": "https://recherchemedicale.com/mesh/D046768", "about": { "@type": "MedicalCondition", "name": "Nésidioblastose", "code": { "@type": "MedicalCode", "code": "D046768", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.200.500" } } }, { "@type": "MedicalWebPage", "name": "Coma insulinique", "alternateName": "Insulin Coma", "url": "https://recherchemedicale.com/mesh/D007331", "about": { "@type": "MedicalCondition", "name": "Coma insulinique", "code": { "@type": "MedicalCode", "code": "D007331", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.394.984.492" } } }, { "@type": "MedicalWebPage", "name": "Troubles du métabolisme du fer", "alternateName": "Iron Metabolism Disorders", "url": "https://recherchemedicale.com/mesh/D019189", "about": { "@type": "MedicalCondition", "name": "Troubles du métabolisme du fer", "code": { "@type": "MedicalCode", "code": "D019189", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperferritinémie", "alternateName": "Hyperferritinemia", "url": "https://recherchemedicale.com/mesh/D000085583", "about": { "@type": "MedicalCondition", "name": "Hyperferritinémie", "code": { "@type": "MedicalCode", "code": "D000085583", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.300" } } }, { "@type": "MedicalWebPage", "name": "Carences en fer", "alternateName": "Iron Deficiencies", "url": "https://recherchemedicale.com/mesh/D000090463", "about": { "@type": "MedicalCondition", "name": "Carences en fer", "code": { "@type": "MedicalCode", "code": "D000090463", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie par carence en fer", "alternateName": "Anemia, Iron-Deficiency", "url": "https://recherchemedicale.com/mesh/D018798", "about": { "@type": "MedicalCondition", "name": "Anémie par carence en fer", "code": { "@type": "MedicalCode", "code": "D018798", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie par carence en fer", "alternateName": "Anemia, Iron-Deficiency", "url": "https://recherchemedicale.com/mesh/D018798", "about": { "@type": "MedicalCondition", "name": "Anémie par carence en fer", "code": { "@type": "MedicalCode", "code": "D018798", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400.500" } } }, { "@type": "MedicalWebPage", "name": "Surcharge en fer", "alternateName": "Iron Overload", "url": "https://recherchemedicale.com/mesh/D019190", "about": { "@type": "MedicalCondition", "name": "Surcharge en fer", "code": { "@type": "MedicalCode", "code": "D019190", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hémosidérose", "alternateName": "Hemosiderosis", "url": "https://recherchemedicale.com/mesh/D006486", "about": { "@type": "MedicalCondition", "name": "Hémosidérose", "code": { "@type": "MedicalCode", "code": "D006486", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hémosidérose", "alternateName": "Hemosiderosis", "url": "https://recherchemedicale.com/mesh/D006486", "about": { "@type": "MedicalCondition", "name": "Hémosidérose", "code": { "@type": "MedicalCode", "code": "D006486", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperferritinémie", "alternateName": "Hyperferritinemia", "url": "https://recherchemedicale.com/mesh/D000085583", "about": { "@type": "MedicalCondition", "name": "Hyperferritinémie", "code": { "@type": "MedicalCode", "code": "D000085583", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.300" } } }, { "@type": "MedicalWebPage", "name": "Carences en fer", "alternateName": "Iron Deficiencies", "url": "https://recherchemedicale.com/mesh/D000090463", "about": { "@type": "MedicalCondition", "name": "Carences en fer", "code": { "@type": "MedicalCode", "code": "D000090463", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie par carence en fer", "alternateName": "Anemia, Iron-Deficiency", "url": "https://recherchemedicale.com/mesh/D018798", "about": { "@type": "MedicalCondition", "name": "Anémie par carence en fer", "code": { "@type": "MedicalCode", "code": "D018798", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie par carence en fer", "alternateName": "Anemia, Iron-Deficiency", "url": "https://recherchemedicale.com/mesh/D018798", "about": { "@type": "MedicalCondition", "name": "Anémie par carence en fer", "code": { "@type": "MedicalCode", "code": "D018798", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.400.500" } } }, { "@type": "MedicalWebPage", "name": "Surcharge en fer", "alternateName": "Iron Overload", "url": "https://recherchemedicale.com/mesh/D019190", "about": { "@type": "MedicalCondition", "name": "Surcharge en fer", "code": { "@type": "MedicalCode", "code": "D019190", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hémosidérose", "alternateName": "Hemosiderosis", "url": "https://recherchemedicale.com/mesh/D006486", "about": { "@type": "MedicalCondition", "name": "Hémosidérose", "code": { "@type": "MedicalCode", "code": "D006486", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hémosidérose", "alternateName": "Hemosiderosis", "url": "https://recherchemedicale.com/mesh/D006486", "about": { "@type": "MedicalCondition", "name": "Hémosidérose", "code": { "@type": "MedicalCode", "code": "D006486", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.565.500.500" } } }, { "@type": "MedicalWebPage", "name": "Troubles du métabolisme lipidique", "alternateName": "Lipid Metabolism Disorders", "url": "https://recherchemedicale.com/mesh/D052439", "about": { "@type": "MedicalCondition", "name": "Troubles du métabolisme lipidique", "code": { "@type": "MedicalCode", "code": "D052439", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Dyslipidémies", "alternateName": "Dyslipidemias", "url": "https://recherchemedicale.com/mesh/D050171", "about": { "@type": "MedicalCondition", "name": "Dyslipidémies", "code": { "@type": "MedicalCode", "code": "D050171", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperlipidémies", "alternateName": "Hyperlipidemias", "url": "https://recherchemedicale.com/mesh/D006949", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémies", "code": { "@type": "MedicalCode", "code": "D006949", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperlipidémies", "alternateName": "Hyperlipidemias", "url": "https://recherchemedicale.com/mesh/D006949", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémies", "code": { "@type": "MedicalCode", "code": "D006949", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémie familiale", "alternateName": "Hypobetalipoproteinemia, Familial, Apolipoprotein B", "url": "https://recherchemedicale.com/mesh/D052476", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémie familiale", "code": { "@type": "MedicalCode", "code": "D052476", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.563.497" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose", "alternateName": "Lipomatosis", "url": "https://recherchemedicale.com/mesh/D008068", "about": { "@type": "MedicalCondition", "name": "Lipomatose", "code": { "@type": "MedicalCode", "code": "D008068", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Adipose douloureuse", "alternateName": "Adiposis Dolorosa", "url": "https://recherchemedicale.com/mesh/D000274", "about": { "@type": "MedicalCondition", "name": "Adipose douloureuse", "code": { "@type": "MedicalCode", "code": "D000274", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.500" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose familiale", "alternateName": "Familial Multiple Lipomatosis", "url": "https://recherchemedicale.com/mesh/D000071070", "about": { "@type": "MedicalCondition", "name": "Lipomatose familiale", "code": { "@type": "MedicalCode", "code": "D000071070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.625" } } }, { "@type": "MedicalWebPage", "name": "Adénolipomatose symétrique à prédominance cervicale", "alternateName": "Lipomatosis, Multiple Symmetrical", "url": "https://recherchemedicale.com/mesh/D008069", "about": { "@type": "MedicalCondition", "name": "Adénolipomatose symétrique à prédominance cervicale", "code": { "@type": "MedicalCode", "code": "D008069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Shwachman", "alternateName": "Shwachman-Diamond Syndrome", "url": "https://recherchemedicale.com/mesh/D000081003", "about": { "@type": "MedicalCondition", "name": "Maladie de Shwachman", "code": { "@type": "MedicalCode", "code": "D000081003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Adipose douloureuse", "alternateName": "Adiposis Dolorosa", "url": "https://recherchemedicale.com/mesh/D000274", "about": { "@type": "MedicalCondition", "name": "Adipose douloureuse", "code": { "@type": "MedicalCode", "code": "D000274", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.500" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose familiale", "alternateName": "Familial Multiple Lipomatosis", "url": "https://recherchemedicale.com/mesh/D000071070", "about": { "@type": "MedicalCondition", "name": "Lipomatose familiale", "code": { "@type": "MedicalCode", "code": "D000071070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.625" } } }, { "@type": "MedicalWebPage", "name": "Adénolipomatose symétrique à prédominance cervicale", "alternateName": "Lipomatosis, Multiple Symmetrical", "url": "https://recherchemedicale.com/mesh/D008069", "about": { "@type": "MedicalCondition", "name": "Adénolipomatose symétrique à prédominance cervicale", "code": { "@type": "MedicalCode", "code": "D008069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Shwachman", "alternateName": "Shwachman-Diamond Syndrome", "url": "https://recherchemedicale.com/mesh/D000081003", "about": { "@type": "MedicalCondition", "name": "Maladie de Shwachman", "code": { "@type": "MedicalCode", "code": "D000081003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.875" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose", "alternateName": "Xanthomatosis", "url": "https://recherchemedicale.com/mesh/D014973", "about": { "@type": "MedicalCondition", "name": "Xanthomatose", "code": { "@type": "MedicalCode", "code": "D014973", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Dyslipidémies", "alternateName": "Dyslipidemias", "url": "https://recherchemedicale.com/mesh/D050171", "about": { "@type": "MedicalCondition", "name": "Dyslipidémies", "code": { "@type": "MedicalCode", "code": "D050171", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperlipidémies", "alternateName": "Hyperlipidemias", "url": "https://recherchemedicale.com/mesh/D006949", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémies", "code": { "@type": "MedicalCode", "code": "D006949", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperlipidémies", "alternateName": "Hyperlipidemias", "url": "https://recherchemedicale.com/mesh/D006949", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémies", "code": { "@type": "MedicalCode", "code": "D006949", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie", "alternateName": "Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D006937", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie", "code": { "@type": "MedicalCode", "code": "D006937", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.396" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémies", "alternateName": "Hyperlipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006951", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006951", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.644" } } }, { "@type": "MedicalWebPage", "name": "Hypertriglycéridémie", "alternateName": "Hypertriglyceridemia", "url": "https://recherchemedicale.com/mesh/D015228", "about": { "@type": "MedicalCondition", "name": "Hypertriglycéridémie", "code": { "@type": "MedicalCode", "code": "D015228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.500.500.851" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémie familiale", "alternateName": "Hypobetalipoproteinemia, Familial, Apolipoprotein B", "url": "https://recherchemedicale.com/mesh/D052476", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémie familiale", "code": { "@type": "MedicalCode", "code": "D052476", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.563.497" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose", "alternateName": "Lipomatosis", "url": "https://recherchemedicale.com/mesh/D008068", "about": { "@type": "MedicalCondition", "name": "Lipomatose", "code": { "@type": "MedicalCode", "code": "D008068", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Adipose douloureuse", "alternateName": "Adiposis Dolorosa", "url": "https://recherchemedicale.com/mesh/D000274", "about": { "@type": "MedicalCondition", "name": "Adipose douloureuse", "code": { "@type": "MedicalCode", "code": "D000274", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.500" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose familiale", "alternateName": "Familial Multiple Lipomatosis", "url": "https://recherchemedicale.com/mesh/D000071070", "about": { "@type": "MedicalCondition", "name": "Lipomatose familiale", "code": { "@type": "MedicalCode", "code": "D000071070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.625" } } }, { "@type": "MedicalWebPage", "name": "Adénolipomatose symétrique à prédominance cervicale", "alternateName": "Lipomatosis, Multiple Symmetrical", "url": "https://recherchemedicale.com/mesh/D008069", "about": { "@type": "MedicalCondition", "name": "Adénolipomatose symétrique à prédominance cervicale", "code": { "@type": "MedicalCode", "code": "D008069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Shwachman", "alternateName": "Shwachman-Diamond Syndrome", "url": "https://recherchemedicale.com/mesh/D000081003", "about": { "@type": "MedicalCondition", "name": "Maladie de Shwachman", "code": { "@type": "MedicalCode", "code": "D000081003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Adipose douloureuse", "alternateName": "Adiposis Dolorosa", "url": "https://recherchemedicale.com/mesh/D000274", "about": { "@type": "MedicalCondition", "name": "Adipose douloureuse", "code": { "@type": "MedicalCode", "code": "D000274", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.500" } } }, { "@type": "MedicalWebPage", "name": "Lipomatose familiale", "alternateName": "Familial Multiple Lipomatosis", "url": "https://recherchemedicale.com/mesh/D000071070", "about": { "@type": "MedicalCondition", "name": "Lipomatose familiale", "code": { "@type": "MedicalCode", "code": "D000071070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.625" } } }, { "@type": "MedicalWebPage", "name": "Adénolipomatose symétrique à prédominance cervicale", "alternateName": "Lipomatosis, Multiple Symmetrical", "url": "https://recherchemedicale.com/mesh/D008069", "about": { "@type": "MedicalCondition", "name": "Adénolipomatose symétrique à prédominance cervicale", "code": { "@type": "MedicalCode", "code": "D008069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Shwachman", "alternateName": "Shwachman-Diamond Syndrome", "url": "https://recherchemedicale.com/mesh/D000081003", "about": { "@type": "MedicalCondition", "name": "Maladie de Shwachman", "code": { "@type": "MedicalCode", "code": "D000081003", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.718.875" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose", "alternateName": "Xanthomatosis", "url": "https://recherchemedicale.com/mesh/D014973", "about": { "@type": "MedicalCondition", "name": "Xanthomatose", "code": { "@type": "MedicalCode", "code": "D014973", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.584.750" } } }, { "@type": "MedicalWebPage", "name": "Syndromes de malabsorption", "alternateName": "Malabsorption Syndromes", "url": "https://recherchemedicale.com/mesh/D008286", "about": { "@type": "MedicalCondition", "name": "Syndromes de malabsorption", "code": { "@type": "MedicalCode", "code": "D008286", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de l'anse borgne", "alternateName": "Blind Loop Syndrome", "url": "https://recherchemedicale.com/mesh/D001765", "about": { "@type": "MedicalCondition", "name": "Syndrome de l'anse borgne", "code": { "@type": "MedicalCode", "code": "D001765", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.145" } } }, { "@type": "MedicalWebPage", "name": "Maladie coeliaque", "alternateName": "Celiac Disease", "url": "https://recherchemedicale.com/mesh/D002446", "about": { "@type": "MedicalCondition", "name": "Maladie coeliaque", "code": { "@type": "MedicalCode", "code": "D002446", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.250" } } }, { "@type": "MedicalWebPage", "name": "Sprue collagène", "alternateName": "Collagenous Sprue", "url": "https://recherchemedicale.com/mesh/D064068", "about": { "@type": "MedicalCondition", "name": "Sprue collagène", "code": { "@type": "MedicalCode", "code": "D064068", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.314" } } }, { "@type": "MedicalWebPage", "name": "Sprue tropicale", "alternateName": "Sprue, Tropical", "url": "https://recherchemedicale.com/mesh/D013182", "about": { "@type": "MedicalCondition", "name": "Sprue tropicale", "code": { "@type": "MedicalCode", "code": "D013182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.850" } } }, { "@type": "MedicalWebPage", "name": "Stéatorrhée", "alternateName": "Steatorrhea", "url": "https://recherchemedicale.com/mesh/D045602", "about": { "@type": "MedicalCondition", "name": "Stéatorrhée", "code": { "@type": "MedicalCode", "code": "D045602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.887" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Whipple", "alternateName": "Whipple Disease", "url": "https://recherchemedicale.com/mesh/D008061", "about": { "@type": "MedicalCondition", "name": "Maladie de Whipple", "code": { "@type": "MedicalCode", "code": "D008061", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.925" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de l'anse borgne", "alternateName": "Blind Loop Syndrome", "url": "https://recherchemedicale.com/mesh/D001765", "about": { "@type": "MedicalCondition", "name": "Syndrome de l'anse borgne", "code": { "@type": "MedicalCode", "code": "D001765", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.145" } } }, { "@type": "MedicalWebPage", "name": "Maladie coeliaque", "alternateName": "Celiac Disease", "url": "https://recherchemedicale.com/mesh/D002446", "about": { "@type": "MedicalCondition", "name": "Maladie coeliaque", "code": { "@type": "MedicalCode", "code": "D002446", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.250" } } }, { "@type": "MedicalWebPage", "name": "Sprue collagène", "alternateName": "Collagenous Sprue", "url": "https://recherchemedicale.com/mesh/D064068", "about": { "@type": "MedicalCondition", "name": "Sprue collagène", "code": { "@type": "MedicalCode", "code": "D064068", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.314" } } }, { "@type": "MedicalWebPage", "name": "Sprue tropicale", "alternateName": "Sprue, Tropical", "url": "https://recherchemedicale.com/mesh/D013182", "about": { "@type": "MedicalCondition", "name": "Sprue tropicale", "code": { "@type": "MedicalCode", "code": "D013182", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.850" } } }, { "@type": "MedicalWebPage", "name": "Stéatorrhée", "alternateName": "Steatorrhea", "url": "https://recherchemedicale.com/mesh/D045602", "about": { "@type": "MedicalCondition", "name": "Stéatorrhée", "code": { "@type": "MedicalCode", "code": "D045602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.887" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Whipple", "alternateName": "Whipple Disease", "url": "https://recherchemedicale.com/mesh/D008061", "about": { "@type": "MedicalCondition", "name": "Maladie de Whipple", "code": { "@type": "MedicalCode", "code": "D008061", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.603.925" } } }, { "@type": "MedicalWebPage", "name": "Syndrome métabolique X", "alternateName": "Metabolic Syndrome", "url": "https://recherchemedicale.com/mesh/D024821", "about": { "@type": "MedicalCondition", "name": "Syndrome métabolique X", "code": { "@type": "MedicalCode", "code": "D024821", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.625" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme", "alternateName": "Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D008661", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme", "code": { "@type": "MedicalCode", "code": "D008661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Aminoacidopathies congénitales", "alternateName": "Amino Acid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D000592", "about": { "@type": "MedicalCondition", "name": "Aminoacidopathies congénitales", "code": { "@type": "MedicalCode", "code": "D000592", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme", "alternateName": "Albinism", "url": "https://recherchemedicale.com/mesh/D000417", "about": { "@type": "MedicalCondition", "name": "Albinisme", "code": { "@type": "MedicalCode", "code": "D000417", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } }, { "@type": "MedicalWebPage", "name": "Alcaptonurie", "alternateName": "Alkaptonuria", "url": "https://recherchemedicale.com/mesh/D000474", "about": { "@type": "MedicalCondition", "name": "Alcaptonurie", "code": { "@type": "MedicalCode", "code": "D000474", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.187" } } }, { "@type": "MedicalWebPage", "name": "Acidémie propionique", "alternateName": "Propionic Acidemia", "url": "https://recherchemedicale.com/mesh/D056693", "about": { "@type": "MedicalCondition", "name": "Acidémie propionique", "code": { "@type": "MedicalCode", "code": "D056693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.823" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme", "alternateName": "Albinism", "url": "https://recherchemedicale.com/mesh/D000417", "about": { "@type": "MedicalCondition", "name": "Albinisme", "code": { "@type": "MedicalCode", "code": "D000417", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } }, { "@type": "MedicalWebPage", "name": "Alcaptonurie", "alternateName": "Alkaptonuria", "url": "https://recherchemedicale.com/mesh/D000474", "about": { "@type": "MedicalCondition", "name": "Alcaptonurie", "code": { "@type": "MedicalCode", "code": "D000474", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.187" } } }, { "@type": "MedicalWebPage", "name": "Acidémie propionique", "alternateName": "Propionic Acidemia", "url": "https://recherchemedicale.com/mesh/D056693", "about": { "@type": "MedicalCondition", "name": "Acidémie propionique", "code": { "@type": "MedicalCode", "code": "D056693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.823" } } }, { "@type": "MedicalWebPage", "name": "Troubles congénitaux du transport des acides aminés", "alternateName": "Amino Acid Transport Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D020157", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux du transport des acides aminés", "code": { "@type": "MedicalCode", "code": "D020157", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.151" } } }, { "@type": "MedicalWebPage", "name": "Encéphalopathies métaboliques congénitales", "alternateName": "Brain Diseases, Metabolic, Inborn", "url": "https://recherchemedicale.com/mesh/D020739", "about": { "@type": "MedicalCondition", "name": "Encéphalopathies métaboliques congénitales", "code": { "@type": "MedicalCode", "code": "D020739", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Hartnup", "alternateName": "Hartnup Disease", "url": "https://recherchemedicale.com/mesh/D006250", "about": { "@type": "MedicalCondition", "name": "Maladie de Hartnup", "code": { "@type": "MedicalCode", "code": "D006250", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.355" } } }, { "@type": "MedicalWebPage", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "alternateName": "Hereditary Central Nervous System Demyelinating Diseases", "url": "https://recherchemedicale.com/mesh/D020279", "about": { "@type": "MedicalCondition", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "code": { "@type": "MedicalCode", "code": "D020279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } }, { "@type": "MedicalWebPage", "name": "Homocystinurie", "alternateName": "Homocystinuria", "url": "https://recherchemedicale.com/mesh/D006712", "about": { "@type": "MedicalCondition", "name": "Homocystinurie", "code": { "@type": "MedicalCode", "code": "D006712", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.365" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycinémie non cétosique", "alternateName": "Hyperglycinemia, Nonketotic", "url": "https://recherchemedicale.com/mesh/D020158", "about": { "@type": "MedicalCondition", "name": "Hyperglycinémie non cétosique", "code": { "@type": "MedicalCode", "code": "D020158", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.375" } } }, { "@type": "MedicalWebPage", "name": "Hyperlysinémies", "alternateName": "Hyperlysinemias", "url": "https://recherchemedicale.com/mesh/D020167", "about": { "@type": "MedicalCondition", "name": "Hyperlysinémies", "code": { "@type": "MedicalCode", "code": "D020167", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.380" } } }, { "@type": "MedicalWebPage", "name": "Leucinose", "alternateName": "Maple Syrup Urine Disease", "url": "https://recherchemedicale.com/mesh/D008375", "about": { "@type": "MedicalCondition", "name": "Leucinose", "code": { "@type": "MedicalCode", "code": "D008375", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lowe", "alternateName": "Oculocerebrorenal Syndrome", "url": "https://recherchemedicale.com/mesh/D009800", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lowe", "code": { "@type": "MedicalCode", "code": "D009800", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.640" } } }, { "@type": "MedicalWebPage", "name": "Phénylcétonuries", "alternateName": "Phenylketonurias", "url": "https://recherchemedicale.com/mesh/D010661", "about": { "@type": "MedicalCondition", "name": "Phénylcétonuries", "code": { "@type": "MedicalCode", "code": "D010661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } }, { "@type": "MedicalWebPage", "name": "Tyrosinémies", "alternateName": "Tyrosinemias", "url": "https://recherchemedicale.com/mesh/D020176", "about": { "@type": "MedicalCondition", "name": "Tyrosinémies", "code": { "@type": "MedicalCode", "code": "D020176", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.875" } } }, { "@type": "MedicalWebPage", "name": "Anomalies congénitales du cycle de l'urée", "alternateName": "Urea Cycle Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D056806", "about": { "@type": "MedicalCondition", "name": "Anomalies congénitales du cycle de l'urée", "code": { "@type": "MedicalCode", "code": "D056806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Hartnup", "alternateName": "Hartnup Disease", "url": "https://recherchemedicale.com/mesh/D006250", "about": { "@type": "MedicalCondition", "name": "Maladie de Hartnup", "code": { "@type": "MedicalCode", "code": "D006250", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.355" } } }, { "@type": "MedicalWebPage", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "alternateName": "Hereditary Central Nervous System Demyelinating Diseases", "url": "https://recherchemedicale.com/mesh/D020279", "about": { "@type": "MedicalCondition", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "code": { "@type": "MedicalCode", "code": "D020279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } }, { "@type": "MedicalWebPage", "name": "Homocystinurie", "alternateName": "Homocystinuria", "url": "https://recherchemedicale.com/mesh/D006712", "about": { "@type": "MedicalCondition", "name": "Homocystinurie", "code": { "@type": "MedicalCode", "code": "D006712", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.365" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycinémie non cétosique", "alternateName": "Hyperglycinemia, Nonketotic", "url": "https://recherchemedicale.com/mesh/D020158", "about": { "@type": "MedicalCondition", "name": "Hyperglycinémie non cétosique", "code": { "@type": "MedicalCode", "code": "D020158", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.375" } } }, { "@type": "MedicalWebPage", "name": "Hyperlysinémies", "alternateName": "Hyperlysinemias", "url": "https://recherchemedicale.com/mesh/D020167", "about": { "@type": "MedicalCondition", "name": "Hyperlysinémies", "code": { "@type": "MedicalCode", "code": "D020167", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.380" } } }, { "@type": "MedicalWebPage", "name": "Leucinose", "alternateName": "Maple Syrup Urine Disease", "url": "https://recherchemedicale.com/mesh/D008375", "about": { "@type": "MedicalCondition", "name": "Leucinose", "code": { "@type": "MedicalCode", "code": "D008375", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lowe", "alternateName": "Oculocerebrorenal Syndrome", "url": "https://recherchemedicale.com/mesh/D009800", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lowe", "code": { "@type": "MedicalCode", "code": "D009800", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.640" } } }, { "@type": "MedicalWebPage", "name": "Phénylcétonuries", "alternateName": "Phenylketonurias", "url": "https://recherchemedicale.com/mesh/D010661", "about": { "@type": "MedicalCondition", "name": "Phénylcétonuries", "code": { "@type": "MedicalCode", "code": "D010661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } }, { "@type": "MedicalWebPage", "name": "Tyrosinémies", "alternateName": "Tyrosinemias", "url": "https://recherchemedicale.com/mesh/D020176", "about": { "@type": "MedicalCondition", "name": "Tyrosinémies", "code": { "@type": "MedicalCode", "code": "D020176", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.875" } } }, { "@type": "MedicalWebPage", "name": "Anomalies congénitales du cycle de l'urée", "alternateName": "Urea Cycle Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D056806", "about": { "@type": "MedicalCondition", "name": "Anomalies congénitales du cycle de l'urée", "code": { "@type": "MedicalCode", "code": "D056806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme glucidique", "alternateName": "Carbohydrate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D002239", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme glucidique", "code": { "@type": "MedicalCode", "code": "D002239", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Troubles congénitaux de la glycosylation", "alternateName": "Congenital Disorders of Glycosylation", "url": "https://recherchemedicale.com/mesh/D018981", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux de la glycosylation", "code": { "@type": "MedicalCode", "code": "D018981", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.125" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du fructose", "alternateName": "Fructose Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015318", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du fructose", "code": { "@type": "MedicalCode", "code": "D015318", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } }, { "@type": "MedicalWebPage", "name": "Galactosémies", "alternateName": "Galactosemias", "url": "https://recherchemedicale.com/mesh/D005693", "about": { "@type": "MedicalCondition", "name": "Galactosémies", "code": { "@type": "MedicalCode", "code": "D005693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.355" } } }, { "@type": "MedicalWebPage", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "alternateName": "Glucosephosphate Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D005955", "about": { "@type": "MedicalCondition", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D005955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.402" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose", "alternateName": "Glycogen Storage Disease", "url": "https://recherchemedicale.com/mesh/D006008", "about": { "@type": "MedicalCondition", "name": "Glycogénose", "code": { "@type": "MedicalCode", "code": "D006008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } }, { "@type": "MedicalWebPage", "name": "Hyperoxalurie primaire", "alternateName": "Hyperoxaluria, Primary", "url": "https://recherchemedicale.com/mesh/D006960", "about": { "@type": "MedicalCondition", "name": "Hyperoxalurie primaire", "code": { "@type": "MedicalCode", "code": "D006960", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.460" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au lactose", "alternateName": "Lactose Intolerance", "url": "https://recherchemedicale.com/mesh/D007787", "about": { "@type": "MedicalCondition", "name": "Intolérance au lactose", "code": { "@type": "MedicalCode", "code": "D007787", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.589" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en carboxylases", "alternateName": "Multiple Carboxylase Deficiency", "url": "https://recherchemedicale.com/mesh/D009100", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en carboxylases", "code": { "@type": "MedicalCode", "code": "D009100", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du pyruvate", "alternateName": "Pyruvate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015323", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du pyruvate", "code": { "@type": "MedicalCode", "code": "D015323", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.810" } } } ] }, { "@type": "MedicalWebPage", "name": "Troubles congénitaux de la glycosylation", "alternateName": "Congenital Disorders of Glycosylation", "url": "https://recherchemedicale.com/mesh/D018981", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux de la glycosylation", "code": { "@type": "MedicalCode", "code": "D018981", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.125" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du fructose", "alternateName": "Fructose Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015318", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du fructose", "code": { "@type": "MedicalCode", "code": "D015318", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } }, { "@type": "MedicalWebPage", "name": "Galactosémies", "alternateName": "Galactosemias", "url": "https://recherchemedicale.com/mesh/D005693", "about": { "@type": "MedicalCondition", "name": "Galactosémies", "code": { "@type": "MedicalCode", "code": "D005693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.355" } } }, { "@type": "MedicalWebPage", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "alternateName": "Glucosephosphate Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D005955", "about": { "@type": "MedicalCondition", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D005955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.402" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose", "alternateName": "Glycogen Storage Disease", "url": "https://recherchemedicale.com/mesh/D006008", "about": { "@type": "MedicalCondition", "name": "Glycogénose", "code": { "@type": "MedicalCode", "code": "D006008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } }, { "@type": "MedicalWebPage", "name": "Hyperoxalurie primaire", "alternateName": "Hyperoxaluria, Primary", "url": "https://recherchemedicale.com/mesh/D006960", "about": { "@type": "MedicalCondition", "name": "Hyperoxalurie primaire", "code": { "@type": "MedicalCode", "code": "D006960", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.460" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au lactose", "alternateName": "Lactose Intolerance", "url": "https://recherchemedicale.com/mesh/D007787", "about": { "@type": "MedicalCondition", "name": "Intolérance au lactose", "code": { "@type": "MedicalCode", "code": "D007787", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.589" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en carboxylases", "alternateName": "Multiple Carboxylase Deficiency", "url": "https://recherchemedicale.com/mesh/D009100", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en carboxylases", "code": { "@type": "MedicalCode", "code": "D009100", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du pyruvate", "alternateName": "Pyruvate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015323", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du pyruvate", "code": { "@type": "MedicalCode", "code": "D015323", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.810" } } }, { "@type": "MedicalWebPage", "name": "Hyperbilirubinémie héréditaire", "alternateName": "Hyperbilirubinemia, Hereditary", "url": "https://recherchemedicale.com/mesh/D006933", "about": { "@type": "MedicalCondition", "name": "Hyperbilirubinémie héréditaire", "code": { "@type": "MedicalCode", "code": "D006933", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de Crigler-Najjar", "alternateName": "Crigler-Najjar Syndrome", "url": "https://recherchemedicale.com/mesh/D003414", "about": { "@type": "MedicalCondition", "name": "Syndrome de Crigler-Najjar", "code": { "@type": "MedicalCode", "code": "D003414", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.281" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gilbert", "alternateName": "Gilbert Disease", "url": "https://recherchemedicale.com/mesh/D005878", "about": { "@type": "MedicalCondition", "name": "Maladie de Gilbert", "code": { "@type": "MedicalCode", "code": "D005878", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.528" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de Crigler-Najjar", "alternateName": "Crigler-Najjar Syndrome", "url": "https://recherchemedicale.com/mesh/D003414", "about": { "@type": "MedicalCondition", "name": "Syndrome de Crigler-Najjar", "code": { "@type": "MedicalCode", "code": "D003414", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.281" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gilbert", "alternateName": "Gilbert Disease", "url": "https://recherchemedicale.com/mesh/D005878", "about": { "@type": "MedicalCondition", "name": "Maladie de Gilbert", "code": { "@type": "MedicalCode", "code": "D005878", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.528" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme lipidique", "alternateName": "Lipid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D008052", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme lipidique", "code": { "@type": "MedicalCode", "code": "D008052", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de Barth", "alternateName": "Barth Syndrome", "url": "https://recherchemedicale.com/mesh/D056889", "about": { "@type": "MedicalCondition", "name": "Syndrome de Barth", "code": { "@type": "MedicalCode", "code": "D056889", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.224" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipidémie familiale mixte", "alternateName": "Hyperlipidemia, Familial Combined", "url": "https://recherchemedicale.com/mesh/D006950", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémie familiale mixte", "code": { "@type": "MedicalCode", "code": "D006950", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type I", "alternateName": "Hyperlipoproteinemia Type I", "url": "https://recherchemedicale.com/mesh/D008072", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type I", "code": { "@type": "MedicalCode", "code": "D008072", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.465" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type II", "alternateName": "Hyperlipoproteinemia Type II", "url": "https://recherchemedicale.com/mesh/D006938", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type II", "code": { "@type": "MedicalCode", "code": "D006938", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type III", "alternateName": "Hyperlipoproteinemia Type III", "url": "https://recherchemedicale.com/mesh/D006952", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type III", "code": { "@type": "MedicalCode", "code": "D006952", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.483" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type IV", "alternateName": "Hyperlipoproteinemia Type IV", "url": "https://recherchemedicale.com/mesh/D006953", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type IV", "code": { "@type": "MedicalCode", "code": "D006953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.487" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type V", "alternateName": "Hyperlipoproteinemia Type V", "url": "https://recherchemedicale.com/mesh/D006954", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type V", "code": { "@type": "MedicalCode", "code": "D006954", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.493" } } }, { "@type": "MedicalWebPage", "name": "Hypolipoprotéinémies", "alternateName": "Hypolipoproteinemias", "url": "https://recherchemedicale.com/mesh/D007009", "about": { "@type": "MedicalCondition", "name": "Hypolipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D007009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } }, { "@type": "MedicalWebPage", "name": "Lipidoses", "alternateName": "Lipidoses", "url": "https://recherchemedicale.com/mesh/D008064", "about": { "@type": "MedicalCondition", "name": "Lipidoses", "code": { "@type": "MedicalCode", "code": "D008064", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } } ] }, { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose cérébrotendineuse", "alternateName": "Xanthomatosis, Cerebrotendinous", "url": "https://recherchemedicale.com/mesh/D019294", "about": { "@type": "MedicalCondition", "name": "Xanthomatose cérébrotendineuse", "code": { "@type": "MedicalCode", "code": "D019294", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.925" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de Barth", "alternateName": "Barth Syndrome", "url": "https://recherchemedicale.com/mesh/D056889", "about": { "@type": "MedicalCondition", "name": "Syndrome de Barth", "code": { "@type": "MedicalCode", "code": "D056889", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.224" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipidémie familiale mixte", "alternateName": "Hyperlipidemia, Familial Combined", "url": "https://recherchemedicale.com/mesh/D006950", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémie familiale mixte", "code": { "@type": "MedicalCode", "code": "D006950", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type I", "alternateName": "Hyperlipoproteinemia Type I", "url": "https://recherchemedicale.com/mesh/D008072", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type I", "code": { "@type": "MedicalCode", "code": "D008072", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.465" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type II", "alternateName": "Hyperlipoproteinemia Type II", "url": "https://recherchemedicale.com/mesh/D006938", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type II", "code": { "@type": "MedicalCode", "code": "D006938", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type III", "alternateName": "Hyperlipoproteinemia Type III", "url": "https://recherchemedicale.com/mesh/D006952", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type III", "code": { "@type": "MedicalCode", "code": "D006952", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.483" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type IV", "alternateName": "Hyperlipoproteinemia Type IV", "url": "https://recherchemedicale.com/mesh/D006953", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type IV", "code": { "@type": "MedicalCode", "code": "D006953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.487" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type V", "alternateName": "Hyperlipoproteinemia Type V", "url": "https://recherchemedicale.com/mesh/D006954", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type V", "code": { "@type": "MedicalCode", "code": "D006954", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.493" } } }, { "@type": "MedicalWebPage", "name": "Hypolipoprotéinémies", "alternateName": "Hypolipoproteinemias", "url": "https://recherchemedicale.com/mesh/D007009", "about": { "@type": "MedicalCondition", "name": "Hypolipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D007009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } }, { "@type": "MedicalWebPage", "name": "Lipidoses", "alternateName": "Lipidoses", "url": "https://recherchemedicale.com/mesh/D008064", "about": { "@type": "MedicalCondition", "name": "Lipidoses", "code": { "@type": "MedicalCode", "code": "D008064", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } } ] }, { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose cérébrotendineuse", "alternateName": "Xanthomatosis, Cerebrotendinous", "url": "https://recherchemedicale.com/mesh/D019294", "about": { "@type": "MedicalCondition", "name": "Xanthomatose cérébrotendineuse", "code": { "@type": "MedicalCode", "code": "D019294", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.925" } } }, { "@type": "MedicalWebPage", "name": "Maladies lysosomiales", "alternateName": "Lysosomal Storage Diseases", "url": "https://recherchemedicale.com/mesh/D016464", "about": { "@type": "MedicalCondition", "name": "Maladies lysosomiales", "code": { "@type": "MedicalCode", "code": "D016464", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Aspartylglucosaminurie", "alternateName": "Aspartylglucosaminuria", "url": "https://recherchemedicale.com/mesh/D054880", "about": { "@type": "MedicalCondition", "name": "Aspartylglucosaminurie", "code": { "@type": "MedicalCode", "code": "D054880", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.100" } } }, { "@type": "MedicalWebPage", "name": "Maladie de stockage des esters de cholestérol", "alternateName": "Cholesterol Ester Storage Disease", "url": "https://recherchemedicale.com/mesh/D015217", "about": { "@type": "MedicalCondition", "name": "Maladie de stockage des esters de cholestérol", "code": { "@type": "MedicalCode", "code": "D015217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } }, { "@type": "MedicalWebPage", "name": "Cystinose", "alternateName": "Cystinosis", "url": "https://recherchemedicale.com/mesh/D003554", "about": { "@type": "MedicalCondition", "name": "Cystinose", "code": { "@type": "MedicalCode", "code": "D003554", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.377" } } }, { "@type": "MedicalWebPage", "name": "Maladies neurologiques de surcharge lysosomiale", "alternateName": "Lysosomal Storage Diseases, Nervous System", "url": "https://recherchemedicale.com/mesh/D020140", "about": { "@type": "MedicalCondition", "name": "Maladies neurologiques de surcharge lysosomiale", "code": { "@type": "MedicalCode", "code": "D020140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } }, { "@type": "MedicalWebPage", "name": "Mannosidoses", "alternateName": "Mannosidase Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D044904", "about": { "@type": "MedicalCondition", "name": "Mannosidoses", "code": { "@type": "MedicalCode", "code": "D044904", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } } ] }, { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidoses", "alternateName": "Mucopolysaccharidoses", "url": "https://recherchemedicale.com/mesh/D009083", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidoses", "code": { "@type": "MedicalCode", "code": "D009083", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } } ] }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } }, { "@type": "MedicalWebPage", "name": "Pycnodysostose", "alternateName": "Pycnodysostosis", "url": "https://recherchemedicale.com/mesh/D058631", "about": { "@type": "MedicalCondition", "name": "Pycnodysostose", "code": { "@type": "MedicalCode", "code": "D058631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.800" } } } ] }, { "@type": "MedicalWebPage", "name": "Aspartylglucosaminurie", "alternateName": "Aspartylglucosaminuria", "url": "https://recherchemedicale.com/mesh/D054880", "about": { "@type": "MedicalCondition", "name": "Aspartylglucosaminurie", "code": { "@type": "MedicalCode", "code": "D054880", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.100" } } }, { "@type": "MedicalWebPage", "name": "Maladie de stockage des esters de cholestérol", "alternateName": "Cholesterol Ester Storage Disease", "url": "https://recherchemedicale.com/mesh/D015217", "about": { "@type": "MedicalCondition", "name": "Maladie de stockage des esters de cholestérol", "code": { "@type": "MedicalCode", "code": "D015217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } }, { "@type": "MedicalWebPage", "name": "Cystinose", "alternateName": "Cystinosis", "url": "https://recherchemedicale.com/mesh/D003554", "about": { "@type": "MedicalCondition", "name": "Cystinose", "code": { "@type": "MedicalCode", "code": "D003554", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.377" } } }, { "@type": "MedicalWebPage", "name": "Maladies neurologiques de surcharge lysosomiale", "alternateName": "Lysosomal Storage Diseases, Nervous System", "url": "https://recherchemedicale.com/mesh/D020140", "about": { "@type": "MedicalCondition", "name": "Maladies neurologiques de surcharge lysosomiale", "code": { "@type": "MedicalCode", "code": "D020140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } }, { "@type": "MedicalWebPage", "name": "Mannosidoses", "alternateName": "Mannosidase Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D044904", "about": { "@type": "MedicalCondition", "name": "Mannosidoses", "code": { "@type": "MedicalCode", "code": "D044904", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } } ] }, { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidoses", "alternateName": "Mucopolysaccharidoses", "url": "https://recherchemedicale.com/mesh/D009083", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidoses", "code": { "@type": "MedicalCode", "code": "D009083", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } } ] }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } }, { "@type": "MedicalWebPage", "name": "Pycnodysostose", "alternateName": "Pycnodysostosis", "url": "https://recherchemedicale.com/mesh/D058631", "about": { "@type": "MedicalCondition", "name": "Pycnodysostose", "code": { "@type": "MedicalCode", "code": "D058631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.800" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme des métaux", "alternateName": "Metal Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D008664", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme des métaux", "code": { "@type": "MedicalCode", "code": "D008664", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hémochromatose", "alternateName": "Hemochromatosis", "url": "https://recherchemedicale.com/mesh/D006432", "about": { "@type": "MedicalCondition", "name": "Hémochromatose", "code": { "@type": "MedicalCode", "code": "D006432", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.337" } } }, { "@type": "MedicalWebPage", "name": "Dégénérescence hépatolenticulaire", "alternateName": "Hepatolenticular Degeneration", "url": "https://recherchemedicale.com/mesh/D006527", "about": { "@type": "MedicalCondition", "name": "Dégénérescence hépatolenticulaire", "code": { "@type": "MedicalCode", "code": "D006527", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.403" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatasie", "alternateName": "Hypophosphatasia", "url": "https://recherchemedicale.com/mesh/D007014", "about": { "@type": "MedicalCondition", "name": "Hypophosphatasie", "code": { "@type": "MedicalCode", "code": "D007014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.482" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Menkès", "alternateName": "Menkes Kinky Hair Syndrome", "url": "https://recherchemedicale.com/mesh/D007706", "about": { "@type": "MedicalCondition", "name": "Maladie de Menkès", "code": { "@type": "MedicalCode", "code": "D007706", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.590" } } }, { "@type": "MedicalWebPage", "name": "Paralysies périodiques familiales", "alternateName": "Paralyses, Familial Periodic", "url": "https://recherchemedicale.com/mesh/D010245", "about": { "@type": "MedicalCondition", "name": "Paralysies périodiques familiales", "code": { "@type": "MedicalCode", "code": "D010245", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } }, { "@type": "MedicalWebPage", "name": "Pseudohypoparathyroïdie", "alternateName": "Pseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011547", "about": { "@type": "MedicalCondition", "name": "Pseudohypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011547", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Hémochromatose", "alternateName": "Hemochromatosis", "url": "https://recherchemedicale.com/mesh/D006432", "about": { "@type": "MedicalCondition", "name": "Hémochromatose", "code": { "@type": "MedicalCode", "code": "D006432", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.337" } } }, { "@type": "MedicalWebPage", "name": "Dégénérescence hépatolenticulaire", "alternateName": "Hepatolenticular Degeneration", "url": "https://recherchemedicale.com/mesh/D006527", "about": { "@type": "MedicalCondition", "name": "Dégénérescence hépatolenticulaire", "code": { "@type": "MedicalCode", "code": "D006527", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.403" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatasie", "alternateName": "Hypophosphatasia", "url": "https://recherchemedicale.com/mesh/D007014", "about": { "@type": "MedicalCondition", "name": "Hypophosphatasie", "code": { "@type": "MedicalCode", "code": "D007014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.482" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Menkès", "alternateName": "Menkes Kinky Hair Syndrome", "url": "https://recherchemedicale.com/mesh/D007706", "about": { "@type": "MedicalCondition", "name": "Maladie de Menkès", "code": { "@type": "MedicalCode", "code": "D007706", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.590" } } }, { "@type": "MedicalWebPage", "name": "Paralysies périodiques familiales", "alternateName": "Paralyses, Familial Periodic", "url": "https://recherchemedicale.com/mesh/D010245", "about": { "@type": "MedicalCondition", "name": "Paralysies périodiques familiales", "code": { "@type": "MedicalCode", "code": "D010245", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } }, { "@type": "MedicalWebPage", "name": "Pseudohypoparathyroïdie", "alternateName": "Pseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011547", "about": { "@type": "MedicalCondition", "name": "Pseudohypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011547", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } }, { "@type": "MedicalWebPage", "name": "Maladies péroxysomiales", "alternateName": "Peroxisomal Disorders", "url": "https://recherchemedicale.com/mesh/D018901", "about": { "@type": "MedicalCondition", "name": "Maladies péroxysomiales", "code": { "@type": "MedicalCode", "code": "D018901", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acatalasie", "alternateName": "Acatalasia", "url": "https://recherchemedicale.com/mesh/D020642", "about": { "@type": "MedicalCondition", "name": "Acatalasie", "code": { "@type": "MedicalCode", "code": "D020642", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.050" } } }, { "@type": "MedicalWebPage", "name": "Chondrodysplasie ponctuée rhizomélique", "alternateName": "Chondrodysplasia Punctata, Rhizomelic", "url": "https://recherchemedicale.com/mesh/D018902", "about": { "@type": "MedicalCondition", "name": "Chondrodysplasie ponctuée rhizomélique", "code": { "@type": "MedicalCode", "code": "D018902", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.265" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum", "alternateName": "Refsum Disease", "url": "https://recherchemedicale.com/mesh/D012035", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum", "code": { "@type": "MedicalCode", "code": "D012035", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.760" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum infantile", "alternateName": "Refsum Disease, Infantile", "url": "https://recherchemedicale.com/mesh/D052919", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum infantile", "code": { "@type": "MedicalCode", "code": "D052919", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.865" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Zellweger", "alternateName": "Zellweger Syndrome", "url": "https://recherchemedicale.com/mesh/D015211", "about": { "@type": "MedicalCondition", "name": "Syndrome de Zellweger", "code": { "@type": "MedicalCode", "code": "D015211", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.970" } } } ] }, { "@type": "MedicalWebPage", "name": "Acatalasie", "alternateName": "Acatalasia", "url": "https://recherchemedicale.com/mesh/D020642", "about": { "@type": "MedicalCondition", "name": "Acatalasie", "code": { "@type": "MedicalCode", "code": "D020642", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.050" } } }, { "@type": "MedicalWebPage", "name": "Chondrodysplasie ponctuée rhizomélique", "alternateName": "Chondrodysplasia Punctata, Rhizomelic", "url": "https://recherchemedicale.com/mesh/D018902", "about": { "@type": "MedicalCondition", "name": "Chondrodysplasie ponctuée rhizomélique", "code": { "@type": "MedicalCode", "code": "D018902", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.265" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum", "alternateName": "Refsum Disease", "url": "https://recherchemedicale.com/mesh/D012035", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum", "code": { "@type": "MedicalCode", "code": "D012035", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.760" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum infantile", "alternateName": "Refsum Disease, Infantile", "url": "https://recherchemedicale.com/mesh/D052919", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum infantile", "code": { "@type": "MedicalCode", "code": "D052919", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.865" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Zellweger", "alternateName": "Zellweger Syndrome", "url": "https://recherchemedicale.com/mesh/D015211", "about": { "@type": "MedicalCondition", "name": "Syndrome de Zellweger", "code": { "@type": "MedicalCode", "code": "D015211", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.970" } } }, { "@type": "MedicalWebPage", "name": "Progeria", "alternateName": "Progeria", "url": "https://recherchemedicale.com/mesh/D011371", "about": { "@type": "MedicalCondition", "name": "Progeria", "code": { "@type": "MedicalCode", "code": "D011371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.753" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme de la purine et de la pyrimidine", "alternateName": "Purine-Pyrimidine Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D011686", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme de la purine et de la pyrimidine", "code": { "@type": "MedicalCode", "code": "D011686", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en dihydropyrimidine déshydrogénase", "alternateName": "Dihydropyrimidine Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054067", "about": { "@type": "MedicalCondition", "name": "Déficit en dihydropyrimidine déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054067", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.183" } } }, { "@type": "MedicalWebPage", "name": "Goutte", "alternateName": "Gout", "url": "https://recherchemedicale.com/mesh/D006073", "about": { "@type": "MedicalCondition", "name": "Goutte", "code": { "@type": "MedicalCode", "code": "D006073", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } } ] }, { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lesch-Nyhan", "alternateName": "Lesch-Nyhan Syndrome", "url": "https://recherchemedicale.com/mesh/D007926", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lesch-Nyhan", "code": { "@type": "MedicalCode", "code": "D007926", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.594" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en dihydropyrimidine déshydrogénase", "alternateName": "Dihydropyrimidine Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054067", "about": { "@type": "MedicalCondition", "name": "Déficit en dihydropyrimidine déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054067", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.183" } } }, { "@type": "MedicalWebPage", "name": "Goutte", "alternateName": "Gout", "url": "https://recherchemedicale.com/mesh/D006073", "about": { "@type": "MedicalCondition", "name": "Goutte", "code": { "@type": "MedicalCode", "code": "D006073", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } } ] }, { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lesch-Nyhan", "alternateName": "Lesch-Nyhan Syndrome", "url": "https://recherchemedicale.com/mesh/D007926", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lesch-Nyhan", "code": { "@type": "MedicalCode", "code": "D007926", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.594" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du transport tubulaire rénal", "alternateName": "Renal Tubular Transport, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015499", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du transport tubulaire rénal", "code": { "@type": "MedicalCode", "code": "D015499", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.893" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme des stéroïdes", "alternateName": "Steroid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D043202", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme des stéroïdes", "code": { "@type": "MedicalCode", "code": "D043202", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénotype du syndrome d'Antley-Bixler", "alternateName": "Antley-Bixler Syndrome Phenotype", "url": "https://recherchemedicale.com/mesh/D054882", "about": { "@type": "MedicalCondition", "name": "Phénotype du syndrome d'Antley-Bixler", "code": { "@type": "MedicalCode", "code": "D054882", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.324" } } }, { "@type": "MedicalWebPage", "name": "Ichtyose liée à l'X", "alternateName": "Ichthyosis, X-Linked", "url": "https://recherchemedicale.com/mesh/D016114", "about": { "@type": "MedicalCondition", "name": "Ichtyose liée à l'X", "code": { "@type": "MedicalCode", "code": "D016114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.400" } } }, { "@type": "MedicalWebPage", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "alternateName": "Mineralocorticoid Excess Syndrome, Apparent", "url": "https://recherchemedicale.com/mesh/D043204", "about": { "@type": "MedicalCondition", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "code": { "@type": "MedicalCode", "code": "D043204", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.500" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Smith-Lemli-Optiz", "alternateName": "Smith-Lemli-Opitz Syndrome", "url": "https://recherchemedicale.com/mesh/D019082", "about": { "@type": "MedicalCondition", "name": "Syndrome de Smith-Lemli-Optiz", "code": { "@type": "MedicalCode", "code": "D019082", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénotype du syndrome d'Antley-Bixler", "alternateName": "Antley-Bixler Syndrome Phenotype", "url": "https://recherchemedicale.com/mesh/D054882", "about": { "@type": "MedicalCondition", "name": "Phénotype du syndrome d'Antley-Bixler", "code": { "@type": "MedicalCode", "code": "D054882", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.324" } } }, { "@type": "MedicalWebPage", "name": "Ichtyose liée à l'X", "alternateName": "Ichthyosis, X-Linked", "url": "https://recherchemedicale.com/mesh/D016114", "about": { "@type": "MedicalCondition", "name": "Ichtyose liée à l'X", "code": { "@type": "MedicalCode", "code": "D016114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.400" } } }, { "@type": "MedicalWebPage", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "alternateName": "Mineralocorticoid Excess Syndrome, Apparent", "url": "https://recherchemedicale.com/mesh/D043204", "about": { "@type": "MedicalCondition", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "code": { "@type": "MedicalCode", "code": "D043204", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.500" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Smith-Lemli-Optiz", "alternateName": "Smith-Lemli-Opitz Syndrome", "url": "https://recherchemedicale.com/mesh/D019082", "about": { "@type": "MedicalCondition", "name": "Syndrome de Smith-Lemli-Optiz", "code": { "@type": "MedicalCode", "code": "D019082", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Aminoacidopathies congénitales", "alternateName": "Amino Acid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D000592", "about": { "@type": "MedicalCondition", "name": "Aminoacidopathies congénitales", "code": { "@type": "MedicalCode", "code": "D000592", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme", "alternateName": "Albinism", "url": "https://recherchemedicale.com/mesh/D000417", "about": { "@type": "MedicalCondition", "name": "Albinisme", "code": { "@type": "MedicalCode", "code": "D000417", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } }, { "@type": "MedicalWebPage", "name": "Alcaptonurie", "alternateName": "Alkaptonuria", "url": "https://recherchemedicale.com/mesh/D000474", "about": { "@type": "MedicalCondition", "name": "Alcaptonurie", "code": { "@type": "MedicalCode", "code": "D000474", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.187" } } }, { "@type": "MedicalWebPage", "name": "Acidémie propionique", "alternateName": "Propionic Acidemia", "url": "https://recherchemedicale.com/mesh/D056693", "about": { "@type": "MedicalCondition", "name": "Acidémie propionique", "code": { "@type": "MedicalCode", "code": "D056693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.823" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme", "alternateName": "Albinism", "url": "https://recherchemedicale.com/mesh/D000417", "about": { "@type": "MedicalCondition", "name": "Albinisme", "code": { "@type": "MedicalCode", "code": "D000417", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Albinisme oculaire", "alternateName": "Albinism, Ocular", "url": "https://recherchemedicale.com/mesh/D016117", "about": { "@type": "MedicalCondition", "name": "Albinisme oculaire", "code": { "@type": "MedicalCode", "code": "D016117", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.090" } } }, { "@type": "MedicalWebPage", "name": "Albinisme oculocutané", "alternateName": "Albinism, Oculocutaneous", "url": "https://recherchemedicale.com/mesh/D016115", "about": { "@type": "MedicalCondition", "name": "Albinisme oculocutané", "code": { "@type": "MedicalCode", "code": "D016115", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome d'Hermanski-Pudlak", "alternateName": "Hermanski-Pudlak Syndrome", "url": "https://recherchemedicale.com/mesh/D022861", "about": { "@type": "MedicalCondition", "name": "Syndrome d'Hermanski-Pudlak", "code": { "@type": "MedicalCode", "code": "D022861", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.100.400" } } }, { "@type": "MedicalWebPage", "name": "Piébaldisme", "alternateName": "Piebaldism", "url": "https://recherchemedicale.com/mesh/D016116", "about": { "@type": "MedicalCondition", "name": "Piébaldisme", "code": { "@type": "MedicalCode", "code": "D016116", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.102.600" } } }, { "@type": "MedicalWebPage", "name": "Alcaptonurie", "alternateName": "Alkaptonuria", "url": "https://recherchemedicale.com/mesh/D000474", "about": { "@type": "MedicalCondition", "name": "Alcaptonurie", "code": { "@type": "MedicalCode", "code": "D000474", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.187" } } }, { "@type": "MedicalWebPage", "name": "Acidémie propionique", "alternateName": "Propionic Acidemia", "url": "https://recherchemedicale.com/mesh/D056693", "about": { "@type": "MedicalCondition", "name": "Acidémie propionique", "code": { "@type": "MedicalCode", "code": "D056693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.100.823" } } }, { "@type": "MedicalWebPage", "name": "Troubles congénitaux du transport des acides aminés", "alternateName": "Amino Acid Transport Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D020157", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux du transport des acides aminés", "code": { "@type": "MedicalCode", "code": "D020157", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.151" } } }, { "@type": "MedicalWebPage", "name": "Encéphalopathies métaboliques congénitales", "alternateName": "Brain Diseases, Metabolic, Inborn", "url": "https://recherchemedicale.com/mesh/D020739", "about": { "@type": "MedicalCondition", "name": "Encéphalopathies métaboliques congénitales", "code": { "@type": "MedicalCode", "code": "D020739", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Hartnup", "alternateName": "Hartnup Disease", "url": "https://recherchemedicale.com/mesh/D006250", "about": { "@type": "MedicalCondition", "name": "Maladie de Hartnup", "code": { "@type": "MedicalCode", "code": "D006250", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.355" } } }, { "@type": "MedicalWebPage", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "alternateName": "Hereditary Central Nervous System Demyelinating Diseases", "url": "https://recherchemedicale.com/mesh/D020279", "about": { "@type": "MedicalCondition", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "code": { "@type": "MedicalCode", "code": "D020279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } }, { "@type": "MedicalWebPage", "name": "Homocystinurie", "alternateName": "Homocystinuria", "url": "https://recherchemedicale.com/mesh/D006712", "about": { "@type": "MedicalCondition", "name": "Homocystinurie", "code": { "@type": "MedicalCode", "code": "D006712", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.365" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycinémie non cétosique", "alternateName": "Hyperglycinemia, Nonketotic", "url": "https://recherchemedicale.com/mesh/D020158", "about": { "@type": "MedicalCondition", "name": "Hyperglycinémie non cétosique", "code": { "@type": "MedicalCode", "code": "D020158", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.375" } } }, { "@type": "MedicalWebPage", "name": "Hyperlysinémies", "alternateName": "Hyperlysinemias", "url": "https://recherchemedicale.com/mesh/D020167", "about": { "@type": "MedicalCondition", "name": "Hyperlysinémies", "code": { "@type": "MedicalCode", "code": "D020167", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.380" } } }, { "@type": "MedicalWebPage", "name": "Leucinose", "alternateName": "Maple Syrup Urine Disease", "url": "https://recherchemedicale.com/mesh/D008375", "about": { "@type": "MedicalCondition", "name": "Leucinose", "code": { "@type": "MedicalCode", "code": "D008375", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lowe", "alternateName": "Oculocerebrorenal Syndrome", "url": "https://recherchemedicale.com/mesh/D009800", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lowe", "code": { "@type": "MedicalCode", "code": "D009800", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.640" } } }, { "@type": "MedicalWebPage", "name": "Phénylcétonuries", "alternateName": "Phenylketonurias", "url": "https://recherchemedicale.com/mesh/D010661", "about": { "@type": "MedicalCondition", "name": "Phénylcétonuries", "code": { "@type": "MedicalCode", "code": "D010661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } }, { "@type": "MedicalWebPage", "name": "Tyrosinémies", "alternateName": "Tyrosinemias", "url": "https://recherchemedicale.com/mesh/D020176", "about": { "@type": "MedicalCondition", "name": "Tyrosinémies", "code": { "@type": "MedicalCode", "code": "D020176", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.875" } } }, { "@type": "MedicalWebPage", "name": "Anomalies congénitales du cycle de l'urée", "alternateName": "Urea Cycle Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D056806", "about": { "@type": "MedicalCondition", "name": "Anomalies congénitales du cycle de l'urée", "code": { "@type": "MedicalCode", "code": "D056806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Hartnup", "alternateName": "Hartnup Disease", "url": "https://recherchemedicale.com/mesh/D006250", "about": { "@type": "MedicalCondition", "name": "Maladie de Hartnup", "code": { "@type": "MedicalCode", "code": "D006250", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.355" } } }, { "@type": "MedicalWebPage", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "alternateName": "Hereditary Central Nervous System Demyelinating Diseases", "url": "https://recherchemedicale.com/mesh/D020279", "about": { "@type": "MedicalCondition", "name": "Maladies démyélinisantes héréditaires du système nerveux central", "code": { "@type": "MedicalCode", "code": "D020279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie d'Alexander", "alternateName": "Alexander Disease", "url": "https://recherchemedicale.com/mesh/D038261", "about": { "@type": "MedicalCondition", "name": "Maladie d'Alexander", "code": { "@type": "MedicalCode", "code": "D038261", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.312" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Canavan", "alternateName": "Canavan Disease", "url": "https://recherchemedicale.com/mesh/D017825", "about": { "@type": "MedicalCondition", "name": "Maladie de Canavan", "code": { "@type": "MedicalCode", "code": "D017825", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.375" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Pelizaeus-Merzbacher", "alternateName": "Pelizaeus-Merzbacher Disease", "url": "https://recherchemedicale.com/mesh/D020371", "about": { "@type": "MedicalCondition", "name": "Maladie de Pelizaeus-Merzbacher", "code": { "@type": "MedicalCode", "code": "D020371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.362.775" } } }, { "@type": "MedicalWebPage", "name": "Homocystinurie", "alternateName": "Homocystinuria", "url": "https://recherchemedicale.com/mesh/D006712", "about": { "@type": "MedicalCondition", "name": "Homocystinurie", "code": { "@type": "MedicalCode", "code": "D006712", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.365" } } }, { "@type": "MedicalWebPage", "name": "Hyperglycinémie non cétosique", "alternateName": "Hyperglycinemia, Nonketotic", "url": "https://recherchemedicale.com/mesh/D020158", "about": { "@type": "MedicalCondition", "name": "Hyperglycinémie non cétosique", "code": { "@type": "MedicalCode", "code": "D020158", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.375" } } }, { "@type": "MedicalWebPage", "name": "Hyperlysinémies", "alternateName": "Hyperlysinemias", "url": "https://recherchemedicale.com/mesh/D020167", "about": { "@type": "MedicalCondition", "name": "Hyperlysinémies", "code": { "@type": "MedicalCode", "code": "D020167", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.380" } } }, { "@type": "MedicalWebPage", "name": "Leucinose", "alternateName": "Maple Syrup Urine Disease", "url": "https://recherchemedicale.com/mesh/D008375", "about": { "@type": "MedicalCondition", "name": "Leucinose", "code": { "@type": "MedicalCode", "code": "D008375", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lowe", "alternateName": "Oculocerebrorenal Syndrome", "url": "https://recherchemedicale.com/mesh/D009800", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lowe", "code": { "@type": "MedicalCode", "code": "D009800", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.640" } } }, { "@type": "MedicalWebPage", "name": "Phénylcétonuries", "alternateName": "Phenylketonurias", "url": "https://recherchemedicale.com/mesh/D010661", "about": { "@type": "MedicalCondition", "name": "Phénylcétonuries", "code": { "@type": "MedicalCode", "code": "D010661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénylcétonurie maternelle", "alternateName": "Phenylketonuria, Maternal", "url": "https://recherchemedicale.com/mesh/D017042", "about": { "@type": "MedicalCondition", "name": "Phénylcétonurie maternelle", "code": { "@type": "MedicalCode", "code": "D017042", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.687.500" } } }, { "@type": "MedicalWebPage", "name": "Tyrosinémies", "alternateName": "Tyrosinemias", "url": "https://recherchemedicale.com/mesh/D020176", "about": { "@type": "MedicalCondition", "name": "Tyrosinémies", "code": { "@type": "MedicalCode", "code": "D020176", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.875" } } }, { "@type": "MedicalWebPage", "name": "Anomalies congénitales du cycle de l'urée", "alternateName": "Urea Cycle Disorders, Inborn", "url": "https://recherchemedicale.com/mesh/D056806", "about": { "@type": "MedicalCondition", "name": "Anomalies congénitales du cycle de l'urée", "code": { "@type": "MedicalCode", "code": "D056806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Acidurie arginosuccinique", "alternateName": "Argininosuccinic Aciduria", "url": "https://recherchemedicale.com/mesh/D056807", "about": { "@type": "MedicalCondition", "name": "Acidurie arginosuccinique", "code": { "@type": "MedicalCode", "code": "D056807", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.124" } } }, { "@type": "MedicalWebPage", "name": "Citrullinémie", "alternateName": "Citrullinemia", "url": "https://recherchemedicale.com/mesh/D020159", "about": { "@type": "MedicalCondition", "name": "Citrullinémie", "code": { "@type": "MedicalCode", "code": "D020159", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.374" } } }, { "@type": "MedicalWebPage", "name": "Hyperargininémie", "alternateName": "Hyperargininemia", "url": "https://recherchemedicale.com/mesh/D020162", "about": { "@type": "MedicalCondition", "name": "Hyperargininémie", "code": { "@type": "MedicalCode", "code": "D020162", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.437" } } }, { "@type": "MedicalWebPage", "name": "Déficit en ornithine carbamyl transférase", "alternateName": "Ornithine Carbamoyltransferase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020163", "about": { "@type": "MedicalCondition", "name": "Déficit en ornithine carbamyl transférase", "code": { "@type": "MedicalCode", "code": "D020163", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.189.937.500" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme glucidique", "alternateName": "Carbohydrate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D002239", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme glucidique", "code": { "@type": "MedicalCode", "code": "D002239", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Troubles congénitaux de la glycosylation", "alternateName": "Congenital Disorders of Glycosylation", "url": "https://recherchemedicale.com/mesh/D018981", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux de la glycosylation", "code": { "@type": "MedicalCode", "code": "D018981", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.125" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du fructose", "alternateName": "Fructose Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015318", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du fructose", "code": { "@type": "MedicalCode", "code": "D015318", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } }, { "@type": "MedicalWebPage", "name": "Galactosémies", "alternateName": "Galactosemias", "url": "https://recherchemedicale.com/mesh/D005693", "about": { "@type": "MedicalCondition", "name": "Galactosémies", "code": { "@type": "MedicalCode", "code": "D005693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.355" } } }, { "@type": "MedicalWebPage", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "alternateName": "Glucosephosphate Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D005955", "about": { "@type": "MedicalCondition", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D005955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.402" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose", "alternateName": "Glycogen Storage Disease", "url": "https://recherchemedicale.com/mesh/D006008", "about": { "@type": "MedicalCondition", "name": "Glycogénose", "code": { "@type": "MedicalCode", "code": "D006008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } }, { "@type": "MedicalWebPage", "name": "Hyperoxalurie primaire", "alternateName": "Hyperoxaluria, Primary", "url": "https://recherchemedicale.com/mesh/D006960", "about": { "@type": "MedicalCondition", "name": "Hyperoxalurie primaire", "code": { "@type": "MedicalCode", "code": "D006960", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.460" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au lactose", "alternateName": "Lactose Intolerance", "url": "https://recherchemedicale.com/mesh/D007787", "about": { "@type": "MedicalCondition", "name": "Intolérance au lactose", "code": { "@type": "MedicalCode", "code": "D007787", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.589" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en carboxylases", "alternateName": "Multiple Carboxylase Deficiency", "url": "https://recherchemedicale.com/mesh/D009100", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en carboxylases", "code": { "@type": "MedicalCode", "code": "D009100", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du pyruvate", "alternateName": "Pyruvate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015323", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du pyruvate", "code": { "@type": "MedicalCode", "code": "D015323", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.810" } } } ] }, { "@type": "MedicalWebPage", "name": "Troubles congénitaux de la glycosylation", "alternateName": "Congenital Disorders of Glycosylation", "url": "https://recherchemedicale.com/mesh/D018981", "about": { "@type": "MedicalCondition", "name": "Troubles congénitaux de la glycosylation", "code": { "@type": "MedicalCode", "code": "D018981", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.125" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du fructose", "alternateName": "Fructose Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015318", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du fructose", "code": { "@type": "MedicalCode", "code": "D015318", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en fructose-1,6-diphosphatase", "alternateName": "Fructose-1,6-Diphosphatase Deficiency", "url": "https://recherchemedicale.com/mesh/D015319", "about": { "@type": "MedicalCondition", "name": "Déficit en fructose-1,6-diphosphatase", "code": { "@type": "MedicalCode", "code": "D015319", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.221" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au fructose", "alternateName": "Fructose Intolerance", "url": "https://recherchemedicale.com/mesh/D005633", "about": { "@type": "MedicalCondition", "name": "Intolérance au fructose", "code": { "@type": "MedicalCode", "code": "D005633", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.251.271" } } }, { "@type": "MedicalWebPage", "name": "Galactosémies", "alternateName": "Galactosemias", "url": "https://recherchemedicale.com/mesh/D005693", "about": { "@type": "MedicalCondition", "name": "Galactosémies", "code": { "@type": "MedicalCode", "code": "D005693", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.355" } } }, { "@type": "MedicalWebPage", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "alternateName": "Glucosephosphate Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D005955", "about": { "@type": "MedicalCondition", "name": "Déficit en glucose-6-phosphate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D005955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.402" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose", "alternateName": "Glycogen Storage Disease", "url": "https://recherchemedicale.com/mesh/D006008", "about": { "@type": "MedicalCondition", "name": "Glycogénose", "code": { "@type": "MedicalCode", "code": "D006008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Glycogénose de type I", "alternateName": "Glycogen Storage Disease Type I", "url": "https://recherchemedicale.com/mesh/D005953", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type I", "code": { "@type": "MedicalCode", "code": "D005953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.448" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IIb", "alternateName": "Glycogen Storage Disease Type IIb", "url": "https://recherchemedicale.com/mesh/D052120", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IIb", "code": { "@type": "MedicalCode", "code": "D052120", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.510" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type III", "alternateName": "Glycogen Storage Disease Type III", "url": "https://recherchemedicale.com/mesh/D006010", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type III", "code": { "@type": "MedicalCode", "code": "D006010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.520" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type IV", "alternateName": "Glycogen Storage Disease Type IV", "url": "https://recherchemedicale.com/mesh/D006011", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type IV", "code": { "@type": "MedicalCode", "code": "D006011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.540" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type V", "alternateName": "Glycogen Storage Disease Type V", "url": "https://recherchemedicale.com/mesh/D006012", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type V", "code": { "@type": "MedicalCode", "code": "D006012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.560" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VI", "alternateName": "Glycogen Storage Disease Type VI", "url": "https://recherchemedicale.com/mesh/D006013", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VI", "code": { "@type": "MedicalCode", "code": "D006013", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.580" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VII", "alternateName": "Glycogen Storage Disease Type VII", "url": "https://recherchemedicale.com/mesh/D006014", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VII", "code": { "@type": "MedicalCode", "code": "D006014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.600" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type VIII", "alternateName": "Glycogen Storage Disease Type VIII", "url": "https://recherchemedicale.com/mesh/D006015", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type VIII", "code": { "@type": "MedicalCode", "code": "D006015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.449.620" } } }, { "@type": "MedicalWebPage", "name": "Hyperoxalurie primaire", "alternateName": "Hyperoxaluria, Primary", "url": "https://recherchemedicale.com/mesh/D006960", "about": { "@type": "MedicalCondition", "name": "Hyperoxalurie primaire", "code": { "@type": "MedicalCode", "code": "D006960", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.460" } } }, { "@type": "MedicalWebPage", "name": "Intolérance au lactose", "alternateName": "Lactose Intolerance", "url": "https://recherchemedicale.com/mesh/D007787", "about": { "@type": "MedicalCondition", "name": "Intolérance au lactose", "code": { "@type": "MedicalCode", "code": "D007787", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.589" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en carboxylases", "alternateName": "Multiple Carboxylase Deficiency", "url": "https://recherchemedicale.com/mesh/D009100", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en carboxylases", "code": { "@type": "MedicalCode", "code": "D009100", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en biotinidase", "alternateName": "Biotinidase Deficiency", "url": "https://recherchemedicale.com/mesh/D028921", "about": { "@type": "MedicalCondition", "name": "Déficit en biotinidase", "code": { "@type": "MedicalCode", "code": "D028921", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.100" } } }, { "@type": "MedicalWebPage", "name": "Déficit en holocarboxylase synthétase", "alternateName": "Holocarboxylase Synthetase Deficiency", "url": "https://recherchemedicale.com/mesh/D028922", "about": { "@type": "MedicalCondition", "name": "Déficit en holocarboxylase synthétase", "code": { "@type": "MedicalCode", "code": "D028922", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.720.380" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme du pyruvate", "alternateName": "Pyruvate Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015323", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme du pyruvate", "code": { "@type": "MedicalCode", "code": "D015323", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.202.810" } } }, { "@type": "MedicalWebPage", "name": "Hyperbilirubinémie héréditaire", "alternateName": "Hyperbilirubinemia, Hereditary", "url": "https://recherchemedicale.com/mesh/D006933", "about": { "@type": "MedicalCondition", "name": "Hyperbilirubinémie héréditaire", "code": { "@type": "MedicalCode", "code": "D006933", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de Crigler-Najjar", "alternateName": "Crigler-Najjar Syndrome", "url": "https://recherchemedicale.com/mesh/D003414", "about": { "@type": "MedicalCondition", "name": "Syndrome de Crigler-Najjar", "code": { "@type": "MedicalCode", "code": "D003414", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.281" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gilbert", "alternateName": "Gilbert Disease", "url": "https://recherchemedicale.com/mesh/D005878", "about": { "@type": "MedicalCondition", "name": "Maladie de Gilbert", "code": { "@type": "MedicalCode", "code": "D005878", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.528" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de Crigler-Najjar", "alternateName": "Crigler-Najjar Syndrome", "url": "https://recherchemedicale.com/mesh/D003414", "about": { "@type": "MedicalCondition", "name": "Syndrome de Crigler-Najjar", "code": { "@type": "MedicalCode", "code": "D003414", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.281" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gilbert", "alternateName": "Gilbert Disease", "url": "https://recherchemedicale.com/mesh/D005878", "about": { "@type": "MedicalCondition", "name": "Maladie de Gilbert", "code": { "@type": "MedicalCode", "code": "D005878", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.300.528" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme lipidique", "alternateName": "Lipid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D008052", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme lipidique", "code": { "@type": "MedicalCode", "code": "D008052", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome de Barth", "alternateName": "Barth Syndrome", "url": "https://recherchemedicale.com/mesh/D056889", "about": { "@type": "MedicalCondition", "name": "Syndrome de Barth", "code": { "@type": "MedicalCode", "code": "D056889", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.224" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipidémie familiale mixte", "alternateName": "Hyperlipidemia, Familial Combined", "url": "https://recherchemedicale.com/mesh/D006950", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémie familiale mixte", "code": { "@type": "MedicalCode", "code": "D006950", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type I", "alternateName": "Hyperlipoproteinemia Type I", "url": "https://recherchemedicale.com/mesh/D008072", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type I", "code": { "@type": "MedicalCode", "code": "D008072", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.465" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type II", "alternateName": "Hyperlipoproteinemia Type II", "url": "https://recherchemedicale.com/mesh/D006938", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type II", "code": { "@type": "MedicalCode", "code": "D006938", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type III", "alternateName": "Hyperlipoproteinemia Type III", "url": "https://recherchemedicale.com/mesh/D006952", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type III", "code": { "@type": "MedicalCode", "code": "D006952", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.483" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type IV", "alternateName": "Hyperlipoproteinemia Type IV", "url": "https://recherchemedicale.com/mesh/D006953", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type IV", "code": { "@type": "MedicalCode", "code": "D006953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.487" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type V", "alternateName": "Hyperlipoproteinemia Type V", "url": "https://recherchemedicale.com/mesh/D006954", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type V", "code": { "@type": "MedicalCode", "code": "D006954", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.493" } } }, { "@type": "MedicalWebPage", "name": "Hypolipoprotéinémies", "alternateName": "Hypolipoproteinemias", "url": "https://recherchemedicale.com/mesh/D007009", "about": { "@type": "MedicalCondition", "name": "Hypolipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D007009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } }, { "@type": "MedicalWebPage", "name": "Lipidoses", "alternateName": "Lipidoses", "url": "https://recherchemedicale.com/mesh/D008064", "about": { "@type": "MedicalCondition", "name": "Lipidoses", "code": { "@type": "MedicalCode", "code": "D008064", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } } ] }, { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose cérébrotendineuse", "alternateName": "Xanthomatosis, Cerebrotendinous", "url": "https://recherchemedicale.com/mesh/D019294", "about": { "@type": "MedicalCondition", "name": "Xanthomatose cérébrotendineuse", "code": { "@type": "MedicalCode", "code": "D019294", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.925" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome de Barth", "alternateName": "Barth Syndrome", "url": "https://recherchemedicale.com/mesh/D056889", "about": { "@type": "MedicalCondition", "name": "Syndrome de Barth", "code": { "@type": "MedicalCode", "code": "D056889", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.224" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipidémie familiale mixte", "alternateName": "Hyperlipidemia, Familial Combined", "url": "https://recherchemedicale.com/mesh/D006950", "about": { "@type": "MedicalCondition", "name": "Hyperlipidémie familiale mixte", "code": { "@type": "MedicalCode", "code": "D006950", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.450" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type I", "alternateName": "Hyperlipoproteinemia Type I", "url": "https://recherchemedicale.com/mesh/D008072", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type I", "code": { "@type": "MedicalCode", "code": "D008072", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.465" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type II", "alternateName": "Hyperlipoproteinemia Type II", "url": "https://recherchemedicale.com/mesh/D006938", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type II", "code": { "@type": "MedicalCode", "code": "D006938", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercholestérolémie familiale homozygote", "alternateName": "Homozygous Familial Hypercholesterolemia", "url": "https://recherchemedicale.com/mesh/D000090542", "about": { "@type": "MedicalCondition", "name": "Hypercholestérolémie familiale homozygote", "code": { "@type": "MedicalCode", "code": "D000090542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.481.500" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type III", "alternateName": "Hyperlipoproteinemia Type III", "url": "https://recherchemedicale.com/mesh/D006952", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type III", "code": { "@type": "MedicalCode", "code": "D006952", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.483" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type IV", "alternateName": "Hyperlipoproteinemia Type IV", "url": "https://recherchemedicale.com/mesh/D006953", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type IV", "code": { "@type": "MedicalCode", "code": "D006953", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.487" } } }, { "@type": "MedicalWebPage", "name": "Hyperlipoprotéinémie de type V", "alternateName": "Hyperlipoproteinemia Type V", "url": "https://recherchemedicale.com/mesh/D006954", "about": { "@type": "MedicalCondition", "name": "Hyperlipoprotéinémie de type V", "code": { "@type": "MedicalCode", "code": "D006954", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.493" } } }, { "@type": "MedicalWebPage", "name": "Hypolipoprotéinémies", "alternateName": "Hypolipoproteinemias", "url": "https://recherchemedicale.com/mesh/D007009", "about": { "@type": "MedicalCondition", "name": "Hypolipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D007009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypoalphalipoprotéinémies", "alternateName": "Hypoalphalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D052456", "about": { "@type": "MedicalCondition", "name": "Hypoalphalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D052456", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "alternateName": "Lecithin Cholesterol Acyltransferase Deficiency", "url": "https://recherchemedicale.com/mesh/D007863", "about": { "@type": "MedicalCondition", "name": "Déficit en lécithine-cholestérol-acyl-transférase", "code": { "@type": "MedicalCode", "code": "D007863", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tangier", "alternateName": "Tangier Disease", "url": "https://recherchemedicale.com/mesh/D013631", "about": { "@type": "MedicalCondition", "name": "Maladie de Tangier", "code": { "@type": "MedicalCode", "code": "D013631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.330.750" } } }, { "@type": "MedicalWebPage", "name": "Hypobêtalipoprotéinémies", "alternateName": "Hypobetalipoproteinemias", "url": "https://recherchemedicale.com/mesh/D006995", "about": { "@type": "MedicalCondition", "name": "Hypobêtalipoprotéinémies", "code": { "@type": "MedicalCode", "code": "D006995", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Abêtalipoprotéinémie", "alternateName": "Abetalipoproteinemia", "url": "https://recherchemedicale.com/mesh/D000012", "about": { "@type": "MedicalCondition", "name": "Abêtalipoprotéinémie", "code": { "@type": "MedicalCode", "code": "D000012", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.500.440.500" } } }, { "@type": "MedicalWebPage", "name": "Lipidoses", "alternateName": "Lipidoses", "url": "https://recherchemedicale.com/mesh/D008064", "about": { "@type": "MedicalCondition", "name": "Lipidoses", "code": { "@type": "MedicalCode", "code": "D008064", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } } ] }, { "@type": "MedicalWebPage", "name": "Céroïdes-lipofuscinoses neuronales", "alternateName": "Neuronal Ceroid-Lipofuscinoses", "url": "https://recherchemedicale.com/mesh/D009472", "about": { "@type": "MedicalCondition", "name": "Céroïdes-lipofuscinoses neuronales", "code": { "@type": "MedicalCode", "code": "D009472", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.509" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Sjögren-Larsson", "alternateName": "Sjogren-Larsson Syndrome", "url": "https://recherchemedicale.com/mesh/D016111", "about": { "@type": "MedicalCondition", "name": "Syndrome de Sjögren-Larsson", "code": { "@type": "MedicalCode", "code": "D016111", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.641.723" } } }, { "@type": "MedicalWebPage", "name": "Xanthomatose cérébrotendineuse", "alternateName": "Xanthomatosis, Cerebrotendinous", "url": "https://recherchemedicale.com/mesh/D019294", "about": { "@type": "MedicalCondition", "name": "Xanthomatose cérébrotendineuse", "code": { "@type": "MedicalCode", "code": "D019294", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.398.925" } } }, { "@type": "MedicalWebPage", "name": "Maladies lysosomiales", "alternateName": "Lysosomal Storage Diseases", "url": "https://recherchemedicale.com/mesh/D016464", "about": { "@type": "MedicalCondition", "name": "Maladies lysosomiales", "code": { "@type": "MedicalCode", "code": "D016464", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Aspartylglucosaminurie", "alternateName": "Aspartylglucosaminuria", "url": "https://recherchemedicale.com/mesh/D054880", "about": { "@type": "MedicalCondition", "name": "Aspartylglucosaminurie", "code": { "@type": "MedicalCode", "code": "D054880", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.100" } } }, { "@type": "MedicalWebPage", "name": "Maladie de stockage des esters de cholestérol", "alternateName": "Cholesterol Ester Storage Disease", "url": "https://recherchemedicale.com/mesh/D015217", "about": { "@type": "MedicalCondition", "name": "Maladie de stockage des esters de cholestérol", "code": { "@type": "MedicalCode", "code": "D015217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } }, { "@type": "MedicalWebPage", "name": "Cystinose", "alternateName": "Cystinosis", "url": "https://recherchemedicale.com/mesh/D003554", "about": { "@type": "MedicalCondition", "name": "Cystinose", "code": { "@type": "MedicalCode", "code": "D003554", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.377" } } }, { "@type": "MedicalWebPage", "name": "Maladies neurologiques de surcharge lysosomiale", "alternateName": "Lysosomal Storage Diseases, Nervous System", "url": "https://recherchemedicale.com/mesh/D020140", "about": { "@type": "MedicalCondition", "name": "Maladies neurologiques de surcharge lysosomiale", "code": { "@type": "MedicalCode", "code": "D020140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } }, { "@type": "MedicalWebPage", "name": "Mannosidoses", "alternateName": "Mannosidase Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D044904", "about": { "@type": "MedicalCondition", "name": "Mannosidoses", "code": { "@type": "MedicalCode", "code": "D044904", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } } ] }, { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidoses", "alternateName": "Mucopolysaccharidoses", "url": "https://recherchemedicale.com/mesh/D009083", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidoses", "code": { "@type": "MedicalCode", "code": "D009083", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } } ] }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } }, { "@type": "MedicalWebPage", "name": "Pycnodysostose", "alternateName": "Pycnodysostosis", "url": "https://recherchemedicale.com/mesh/D058631", "about": { "@type": "MedicalCondition", "name": "Pycnodysostose", "code": { "@type": "MedicalCode", "code": "D058631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.800" } } } ] }, { "@type": "MedicalWebPage", "name": "Aspartylglucosaminurie", "alternateName": "Aspartylglucosaminuria", "url": "https://recherchemedicale.com/mesh/D054880", "about": { "@type": "MedicalCondition", "name": "Aspartylglucosaminurie", "code": { "@type": "MedicalCode", "code": "D054880", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.100" } } }, { "@type": "MedicalWebPage", "name": "Maladie de stockage des esters de cholestérol", "alternateName": "Cholesterol Ester Storage Disease", "url": "https://recherchemedicale.com/mesh/D015217", "about": { "@type": "MedicalCondition", "name": "Maladie de stockage des esters de cholestérol", "code": { "@type": "MedicalCode", "code": "D015217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Wolman", "alternateName": "Wolman Disease", "url": "https://recherchemedicale.com/mesh/D015223", "about": { "@type": "MedicalCondition", "name": "Maladie de Wolman", "code": { "@type": "MedicalCode", "code": "D015223", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.201.500" } } }, { "@type": "MedicalWebPage", "name": "Cystinose", "alternateName": "Cystinosis", "url": "https://recherchemedicale.com/mesh/D003554", "about": { "@type": "MedicalCondition", "name": "Cystinose", "code": { "@type": "MedicalCode", "code": "D003554", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.377" } } }, { "@type": "MedicalWebPage", "name": "Maladies neurologiques de surcharge lysosomiale", "alternateName": "Lysosomal Storage Diseases, Nervous System", "url": "https://recherchemedicale.com/mesh/D020140", "about": { "@type": "MedicalCondition", "name": "Maladies neurologiques de surcharge lysosomiale", "code": { "@type": "MedicalCode", "code": "D020140", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Fucosidose", "alternateName": "Fucosidosis", "url": "https://recherchemedicale.com/mesh/D005645", "about": { "@type": "MedicalCondition", "name": "Fucosidose", "code": { "@type": "MedicalCode", "code": "D005645", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.295" } } }, { "@type": "MedicalWebPage", "name": "Glycogénose de type II", "alternateName": "Glycogen Storage Disease Type II", "url": "https://recherchemedicale.com/mesh/D006009", "about": { "@type": "MedicalCondition", "name": "Glycogénose de type II", "code": { "@type": "MedicalCode", "code": "D006009", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.340" } } }, { "@type": "MedicalWebPage", "name": "Mucolipidoses", "alternateName": "Mucolipidoses", "url": "https://recherchemedicale.com/mesh/D009081", "about": { "@type": "MedicalCondition", "name": "Mucolipidoses", "code": { "@type": "MedicalCode", "code": "D009081", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.590" } } }, { "@type": "MedicalWebPage", "name": "Maladie de surcharge en acide sialique", "alternateName": "Sialic Acid Storage Disease", "url": "https://recherchemedicale.com/mesh/D029461", "about": { "@type": "MedicalCondition", "name": "Maladie de surcharge en acide sialique", "code": { "@type": "MedicalCode", "code": "D029461", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.810" } } }, { "@type": "MedicalWebPage", "name": "Sphingolipidoses", "alternateName": "Sphingolipidoses", "url": "https://recherchemedicale.com/mesh/D013106", "about": { "@type": "MedicalCondition", "name": "Sphingolipidoses", "code": { "@type": "MedicalCode", "code": "D013106", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Fabry", "alternateName": "Fabry Disease", "url": "https://recherchemedicale.com/mesh/D000795", "about": { "@type": "MedicalCondition", "name": "Maladie de Fabry", "code": { "@type": "MedicalCode", "code": "D000795", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.200" } } }, { "@type": "MedicalWebPage", "name": "Lipogranulomatose de Farber", "alternateName": "Farber Lipogranulomatosis", "url": "https://recherchemedicale.com/mesh/D055577", "about": { "@type": "MedicalCondition", "name": "Lipogranulomatose de Farber", "code": { "@type": "MedicalCode", "code": "D055577", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.250" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidoses", "alternateName": "Gangliosidoses", "url": "https://recherchemedicale.com/mesh/D005733", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses", "code": { "@type": "MedicalCode", "code": "D005733", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } } ] }, { "@type": "MedicalWebPage", "name": "Gangliosidoses à GM2", "alternateName": "Gangliosidoses, GM2", "url": "https://recherchemedicale.com/mesh/D020143", "about": { "@type": "MedicalCondition", "name": "Gangliosidoses à GM2", "code": { "@type": "MedicalCode", "code": "D020143", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Sandhoff", "alternateName": "Sandhoff Disease", "url": "https://recherchemedicale.com/mesh/D012497", "about": { "@type": "MedicalCondition", "name": "Maladie de Sandhoff", "code": { "@type": "MedicalCode", "code": "D012497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.800" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs", "alternateName": "Tay-Sachs Disease", "url": "https://recherchemedicale.com/mesh/D013661", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs", "code": { "@type": "MedicalCode", "code": "D013661", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.840" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Tay-Sachs variante AB", "alternateName": "Tay-Sachs Disease, AB Variant", "url": "https://recherchemedicale.com/mesh/D049290", "about": { "@type": "MedicalCondition", "name": "Maladie de Tay-Sachs variante AB", "code": { "@type": "MedicalCode", "code": "D049290", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.300.920" } } }, { "@type": "MedicalWebPage", "name": "Gangliosidose à GM1", "alternateName": "Gangliosidosis, GM1", "url": "https://recherchemedicale.com/mesh/D016537", "about": { "@type": "MedicalCondition", "name": "Gangliosidose à GM1", "code": { "@type": "MedicalCode", "code": "D016537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.300.400" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Gaucher", "alternateName": "Gaucher Disease", "url": "https://recherchemedicale.com/mesh/D005776", "about": { "@type": "MedicalCondition", "name": "Maladie de Gaucher", "code": { "@type": "MedicalCode", "code": "D005776", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.400" } } }, { "@type": "MedicalWebPage", "name": "Leucodystrophie à cellules globoïdes", "alternateName": "Leukodystrophy, Globoid Cell", "url": "https://recherchemedicale.com/mesh/D007965", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie à cellules globoïdes", "code": { "@type": "MedicalCode", "code": "D007965", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.590" } } }, { "@type": "MedicalWebPage", "name": "Maladies de Niemann-Pick", "alternateName": "Niemann-Pick Diseases", "url": "https://recherchemedicale.com/mesh/D009542", "about": { "@type": "MedicalCondition", "name": "Maladies de Niemann-Pick", "code": { "@type": "MedicalCode", "code": "D009542", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type A", "alternateName": "Niemann-Pick Disease, Type A", "url": "https://recherchemedicale.com/mesh/D052536", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type A", "code": { "@type": "MedicalCode", "code": "D052536", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.500" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type B", "alternateName": "Niemann-Pick Disease, Type B", "url": "https://recherchemedicale.com/mesh/D052537", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type B", "code": { "@type": "MedicalCode", "code": "D052537", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.750" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Niemann-Pick de type C", "alternateName": "Niemann-Pick Disease, Type C", "url": "https://recherchemedicale.com/mesh/D052556", "about": { "@type": "MedicalCondition", "name": "Maladie de Niemann-Pick de type C", "code": { "@type": "MedicalCode", "code": "D052556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.700.875" } } }, { "@type": "MedicalWebPage", "name": "Syndrome des histiocytes bleus de mer", "alternateName": "Sea-Blue Histiocyte Syndrome", "url": "https://recherchemedicale.com/mesh/D012618", "about": { "@type": "MedicalCondition", "name": "Syndrome des histiocytes bleus de mer", "code": { "@type": "MedicalCode", "code": "D012618", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.775" } } }, { "@type": "MedicalWebPage", "name": "Sulfatidose", "alternateName": "Sulfatidosis", "url": "https://recherchemedicale.com/mesh/D052516", "about": { "@type": "MedicalCondition", "name": "Sulfatidose", "code": { "@type": "MedicalCode", "code": "D052516", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Leucodystrophie métachromatique", "alternateName": "Leukodystrophy, Metachromatic", "url": "https://recherchemedicale.com/mesh/D007966", "about": { "@type": "MedicalCondition", "name": "Leucodystrophie métachromatique", "code": { "@type": "MedicalCode", "code": "D007966", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.500" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en sulfatases", "alternateName": "Multiple Sulfatase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D052517", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en sulfatases", "code": { "@type": "MedicalCode", "code": "D052517", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.554.825.850.750" } } }, { "@type": "MedicalWebPage", "name": "Mannosidoses", "alternateName": "Mannosidase Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D044904", "about": { "@type": "MedicalCondition", "name": "Mannosidoses", "code": { "@type": "MedicalCode", "code": "D044904", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } } ] }, { "@type": "MedicalWebPage", "name": "alpha-Mannosidose", "alternateName": "alpha-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D008363", "about": { "@type": "MedicalCondition", "name": "alpha-Mannosidose", "code": { "@type": "MedicalCode", "code": "D008363", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.500" } } }, { "@type": "MedicalWebPage", "name": "bêta-Mannosidose", "alternateName": "beta-Mannosidosis", "url": "https://recherchemedicale.com/mesh/D044905", "about": { "@type": "MedicalCondition", "name": "bêta-Mannosidose", "code": { "@type": "MedicalCode", "code": "D044905", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.577.750" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidoses", "alternateName": "Mucopolysaccharidoses", "url": "https://recherchemedicale.com/mesh/D009083", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidoses", "code": { "@type": "MedicalCode", "code": "D009083", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } } ] }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type I", "alternateName": "Mucopolysaccharidosis I", "url": "https://recherchemedicale.com/mesh/D008059", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type I", "code": { "@type": "MedicalCode", "code": "D008059", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.640" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type II", "alternateName": "Mucopolysaccharidosis II", "url": "https://recherchemedicale.com/mesh/D016532", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type II", "code": { "@type": "MedicalCode", "code": "D016532", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.645" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type III", "alternateName": "Mucopolysaccharidosis III", "url": "https://recherchemedicale.com/mesh/D009084", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type III", "code": { "@type": "MedicalCode", "code": "D009084", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.650" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type IV", "alternateName": "Mucopolysaccharidosis IV", "url": "https://recherchemedicale.com/mesh/D009085", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type IV", "code": { "@type": "MedicalCode", "code": "D009085", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.655" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VI", "alternateName": "Mucopolysaccharidosis VI", "url": "https://recherchemedicale.com/mesh/D009087", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VI", "code": { "@type": "MedicalCode", "code": "D009087", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.670" } } }, { "@type": "MedicalWebPage", "name": "Mucopolysaccharidose de type VII", "alternateName": "Mucopolysaccharidosis VII", "url": "https://recherchemedicale.com/mesh/D016538", "about": { "@type": "MedicalCondition", "name": "Mucopolysaccharidose de type VII", "code": { "@type": "MedicalCode", "code": "D016538", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.600.675" } } }, { "@type": "MedicalWebPage", "name": "Pycnodysostose", "alternateName": "Pycnodysostosis", "url": "https://recherchemedicale.com/mesh/D058631", "about": { "@type": "MedicalCondition", "name": "Pycnodysostose", "code": { "@type": "MedicalCode", "code": "D058631", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.595.800" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme des métaux", "alternateName": "Metal Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D008664", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme des métaux", "code": { "@type": "MedicalCode", "code": "D008664", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hémochromatose", "alternateName": "Hemochromatosis", "url": "https://recherchemedicale.com/mesh/D006432", "about": { "@type": "MedicalCondition", "name": "Hémochromatose", "code": { "@type": "MedicalCode", "code": "D006432", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.337" } } }, { "@type": "MedicalWebPage", "name": "Dégénérescence hépatolenticulaire", "alternateName": "Hepatolenticular Degeneration", "url": "https://recherchemedicale.com/mesh/D006527", "about": { "@type": "MedicalCondition", "name": "Dégénérescence hépatolenticulaire", "code": { "@type": "MedicalCode", "code": "D006527", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.403" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatasie", "alternateName": "Hypophosphatasia", "url": "https://recherchemedicale.com/mesh/D007014", "about": { "@type": "MedicalCondition", "name": "Hypophosphatasie", "code": { "@type": "MedicalCode", "code": "D007014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.482" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Menkès", "alternateName": "Menkes Kinky Hair Syndrome", "url": "https://recherchemedicale.com/mesh/D007706", "about": { "@type": "MedicalCondition", "name": "Maladie de Menkès", "code": { "@type": "MedicalCode", "code": "D007706", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.590" } } }, { "@type": "MedicalWebPage", "name": "Paralysies périodiques familiales", "alternateName": "Paralyses, Familial Periodic", "url": "https://recherchemedicale.com/mesh/D010245", "about": { "@type": "MedicalCondition", "name": "Paralysies périodiques familiales", "code": { "@type": "MedicalCode", "code": "D010245", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } }, { "@type": "MedicalWebPage", "name": "Pseudohypoparathyroïdie", "alternateName": "Pseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011547", "about": { "@type": "MedicalCondition", "name": "Pseudohypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011547", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Hémochromatose", "alternateName": "Hemochromatosis", "url": "https://recherchemedicale.com/mesh/D006432", "about": { "@type": "MedicalCondition", "name": "Hémochromatose", "code": { "@type": "MedicalCode", "code": "D006432", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.337" } } }, { "@type": "MedicalWebPage", "name": "Dégénérescence hépatolenticulaire", "alternateName": "Hepatolenticular Degeneration", "url": "https://recherchemedicale.com/mesh/D006527", "about": { "@type": "MedicalCondition", "name": "Dégénérescence hépatolenticulaire", "code": { "@type": "MedicalCode", "code": "D006527", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.403" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatasie", "alternateName": "Hypophosphatasia", "url": "https://recherchemedicale.com/mesh/D007014", "about": { "@type": "MedicalCondition", "name": "Hypophosphatasie", "code": { "@type": "MedicalCode", "code": "D007014", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.482" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Menkès", "alternateName": "Menkes Kinky Hair Syndrome", "url": "https://recherchemedicale.com/mesh/D007706", "about": { "@type": "MedicalCondition", "name": "Maladie de Menkès", "code": { "@type": "MedicalCode", "code": "D007706", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.590" } } }, { "@type": "MedicalWebPage", "name": "Paralysies périodiques familiales", "alternateName": "Paralyses, Familial Periodic", "url": "https://recherchemedicale.com/mesh/D010245", "about": { "@type": "MedicalCondition", "name": "Paralysies périodiques familiales", "code": { "@type": "MedicalCode", "code": "D010245", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } } ] }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hypokaliémique", "alternateName": "Hypokalemic Periodic Paralysis", "url": "https://recherchemedicale.com/mesh/D020514", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hypokaliémique", "code": { "@type": "MedicalCode", "code": "D020514", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.550" } } }, { "@type": "MedicalWebPage", "name": "Paralysie périodique hyperkaliémique", "alternateName": "Paralysis, Hyperkalemic Periodic", "url": "https://recherchemedicale.com/mesh/D020513", "about": { "@type": "MedicalCondition", "name": "Paralysie périodique hyperkaliémique", "code": { "@type": "MedicalCode", "code": "D020513", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.711.600" } } }, { "@type": "MedicalWebPage", "name": "Pseudohypoparathyroïdie", "alternateName": "Pseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011547", "about": { "@type": "MedicalCondition", "name": "Pseudohypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011547", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } } ] }, { "@type": "MedicalWebPage", "name": "Pseudopseudo-hypoparathyroïdie", "alternateName": "Pseudopseudohypoparathyroidism", "url": "https://recherchemedicale.com/mesh/D011556", "about": { "@type": "MedicalCondition", "name": "Pseudopseudo-hypoparathyroïdie", "code": { "@type": "MedicalCode", "code": "D011556", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.618.815.815" } } }, { "@type": "MedicalWebPage", "name": "Maladies péroxysomiales", "alternateName": "Peroxisomal Disorders", "url": "https://recherchemedicale.com/mesh/D018901", "about": { "@type": "MedicalCondition", "name": "Maladies péroxysomiales", "code": { "@type": "MedicalCode", "code": "D018901", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Acatalasie", "alternateName": "Acatalasia", "url": "https://recherchemedicale.com/mesh/D020642", "about": { "@type": "MedicalCondition", "name": "Acatalasie", "code": { "@type": "MedicalCode", "code": "D020642", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.050" } } }, { "@type": "MedicalWebPage", "name": "Chondrodysplasie ponctuée rhizomélique", "alternateName": "Chondrodysplasia Punctata, Rhizomelic", "url": "https://recherchemedicale.com/mesh/D018902", "about": { "@type": "MedicalCondition", "name": "Chondrodysplasie ponctuée rhizomélique", "code": { "@type": "MedicalCode", "code": "D018902", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.265" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum", "alternateName": "Refsum Disease", "url": "https://recherchemedicale.com/mesh/D012035", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum", "code": { "@type": "MedicalCode", "code": "D012035", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.760" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum infantile", "alternateName": "Refsum Disease, Infantile", "url": "https://recherchemedicale.com/mesh/D052919", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum infantile", "code": { "@type": "MedicalCode", "code": "D052919", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.865" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Zellweger", "alternateName": "Zellweger Syndrome", "url": "https://recherchemedicale.com/mesh/D015211", "about": { "@type": "MedicalCondition", "name": "Syndrome de Zellweger", "code": { "@type": "MedicalCode", "code": "D015211", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.970" } } } ] }, { "@type": "MedicalWebPage", "name": "Acatalasie", "alternateName": "Acatalasia", "url": "https://recherchemedicale.com/mesh/D020642", "about": { "@type": "MedicalCondition", "name": "Acatalasie", "code": { "@type": "MedicalCode", "code": "D020642", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.050" } } }, { "@type": "MedicalWebPage", "name": "Chondrodysplasie ponctuée rhizomélique", "alternateName": "Chondrodysplasia Punctata, Rhizomelic", "url": "https://recherchemedicale.com/mesh/D018902", "about": { "@type": "MedicalCondition", "name": "Chondrodysplasie ponctuée rhizomélique", "code": { "@type": "MedicalCode", "code": "D018902", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.265" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum", "alternateName": "Refsum Disease", "url": "https://recherchemedicale.com/mesh/D012035", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum", "code": { "@type": "MedicalCode", "code": "D012035", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.760" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Refsum infantile", "alternateName": "Refsum Disease, Infantile", "url": "https://recherchemedicale.com/mesh/D052919", "about": { "@type": "MedicalCondition", "name": "Maladie de Refsum infantile", "code": { "@type": "MedicalCode", "code": "D052919", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.865" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Zellweger", "alternateName": "Zellweger Syndrome", "url": "https://recherchemedicale.com/mesh/D015211", "about": { "@type": "MedicalCondition", "name": "Syndrome de Zellweger", "code": { "@type": "MedicalCode", "code": "D015211", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.663.970" } } }, { "@type": "MedicalWebPage", "name": "Progeria", "alternateName": "Progeria", "url": "https://recherchemedicale.com/mesh/D011371", "about": { "@type": "MedicalCondition", "name": "Progeria", "code": { "@type": "MedicalCode", "code": "D011371", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.753" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme de la purine et de la pyrimidine", "alternateName": "Purine-Pyrimidine Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D011686", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme de la purine et de la pyrimidine", "code": { "@type": "MedicalCode", "code": "D011686", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en dihydropyrimidine déshydrogénase", "alternateName": "Dihydropyrimidine Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054067", "about": { "@type": "MedicalCondition", "name": "Déficit en dihydropyrimidine déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054067", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.183" } } }, { "@type": "MedicalWebPage", "name": "Goutte", "alternateName": "Gout", "url": "https://recherchemedicale.com/mesh/D006073", "about": { "@type": "MedicalCondition", "name": "Goutte", "code": { "@type": "MedicalCode", "code": "D006073", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } } ] }, { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lesch-Nyhan", "alternateName": "Lesch-Nyhan Syndrome", "url": "https://recherchemedicale.com/mesh/D007926", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lesch-Nyhan", "code": { "@type": "MedicalCode", "code": "D007926", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.594" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en dihydropyrimidine déshydrogénase", "alternateName": "Dihydropyrimidine Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054067", "about": { "@type": "MedicalCondition", "name": "Déficit en dihydropyrimidine déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054067", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.183" } } }, { "@type": "MedicalWebPage", "name": "Goutte", "alternateName": "Gout", "url": "https://recherchemedicale.com/mesh/D006073", "about": { "@type": "MedicalCondition", "name": "Goutte", "code": { "@type": "MedicalCode", "code": "D006073", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } } ] }, { "@type": "MedicalWebPage", "name": "Goutte articulaire", "alternateName": "Arthritis, Gouty", "url": "https://recherchemedicale.com/mesh/D015210", "about": { "@type": "MedicalCondition", "name": "Goutte articulaire", "code": { "@type": "MedicalCode", "code": "D015210", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.368.410" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Lesch-Nyhan", "alternateName": "Lesch-Nyhan Syndrome", "url": "https://recherchemedicale.com/mesh/D007926", "about": { "@type": "MedicalCondition", "name": "Syndrome de Lesch-Nyhan", "code": { "@type": "MedicalCode", "code": "D007926", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.798.594" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du transport tubulaire rénal", "alternateName": "Renal Tubular Transport, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D015499", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du transport tubulaire rénal", "code": { "@type": "MedicalCode", "code": "D015499", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.893" } } }, { "@type": "MedicalWebPage", "name": "Erreurs innées du métabolisme des stéroïdes", "alternateName": "Steroid Metabolism, Inborn Errors", "url": "https://recherchemedicale.com/mesh/D043202", "about": { "@type": "MedicalCondition", "name": "Erreurs innées du métabolisme des stéroïdes", "code": { "@type": "MedicalCode", "code": "D043202", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Phénotype du syndrome d'Antley-Bixler", "alternateName": "Antley-Bixler Syndrome Phenotype", "url": "https://recherchemedicale.com/mesh/D054882", "about": { "@type": "MedicalCondition", "name": "Phénotype du syndrome d'Antley-Bixler", "code": { "@type": "MedicalCode", "code": "D054882", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.324" } } }, { "@type": "MedicalWebPage", "name": "Ichtyose liée à l'X", "alternateName": "Ichthyosis, X-Linked", "url": "https://recherchemedicale.com/mesh/D016114", "about": { "@type": "MedicalCondition", "name": "Ichtyose liée à l'X", "code": { "@type": "MedicalCode", "code": "D016114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.400" } } }, { "@type": "MedicalWebPage", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "alternateName": "Mineralocorticoid Excess Syndrome, Apparent", "url": "https://recherchemedicale.com/mesh/D043204", "about": { "@type": "MedicalCondition", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "code": { "@type": "MedicalCode", "code": "D043204", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.500" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Smith-Lemli-Optiz", "alternateName": "Smith-Lemli-Opitz Syndrome", "url": "https://recherchemedicale.com/mesh/D019082", "about": { "@type": "MedicalCondition", "name": "Syndrome de Smith-Lemli-Optiz", "code": { "@type": "MedicalCode", "code": "D019082", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.875" } } } ] }, { "@type": "MedicalWebPage", "name": "Phénotype du syndrome d'Antley-Bixler", "alternateName": "Antley-Bixler Syndrome Phenotype", "url": "https://recherchemedicale.com/mesh/D054882", "about": { "@type": "MedicalCondition", "name": "Phénotype du syndrome d'Antley-Bixler", "code": { "@type": "MedicalCode", "code": "D054882", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.324" } } }, { "@type": "MedicalWebPage", "name": "Ichtyose liée à l'X", "alternateName": "Ichthyosis, X-Linked", "url": "https://recherchemedicale.com/mesh/D016114", "about": { "@type": "MedicalCondition", "name": "Ichtyose liée à l'X", "code": { "@type": "MedicalCode", "code": "D016114", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.400" } } }, { "@type": "MedicalWebPage", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "alternateName": "Mineralocorticoid Excess Syndrome, Apparent", "url": "https://recherchemedicale.com/mesh/D043204", "about": { "@type": "MedicalCondition", "name": "Syndrome d'excès apparent en minéralocorticoïdes", "code": { "@type": "MedicalCode", "code": "D043204", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.500" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Smith-Lemli-Optiz", "alternateName": "Smith-Lemli-Opitz Syndrome", "url": "https://recherchemedicale.com/mesh/D019082", "about": { "@type": "MedicalCondition", "name": "Syndrome de Smith-Lemli-Optiz", "code": { "@type": "MedicalCode", "code": "D019082", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.648.925.875" } } }, { "@type": "MedicalWebPage", "name": "Maladies mitochondriales", "alternateName": "Mitochondrial Diseases", "url": "https://recherchemedicale.com/mesh/D028361", "about": { "@type": "MedicalCondition", "name": "Maladies mitochondriales", "code": { "@type": "MedicalCode", "code": "D028361", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Déficit en carbamoyl-phosphate synthase I", "alternateName": "Carbamoyl-Phosphate Synthase I Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020165", "about": { "@type": "MedicalCondition", "name": "Déficit en carbamoyl-phosphate synthase I", "code": { "@type": "MedicalCode", "code": "D020165", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.097" } } }, { "@type": "MedicalWebPage", "name": "Déficit en cytochrome-c oxydase", "alternateName": "Cytochrome-c Oxidase Deficiency", "url": "https://recherchemedicale.com/mesh/D030401", "about": { "@type": "MedicalCondition", "name": "Déficit en cytochrome-c oxydase", "code": { "@type": "MedicalCode", "code": "D030401", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.195" } } }, { "@type": "MedicalWebPage", "name": "Ataxie de Friedreich", "alternateName": "Friedreich Ataxia", "url": "https://recherchemedicale.com/mesh/D005621", "about": { "@type": "MedicalCondition", "name": "Ataxie de Friedreich", "code": { "@type": "MedicalCode", "code": "D005621", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.300" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Leigh", "alternateName": "Leigh Disease", "url": "https://recherchemedicale.com/mesh/D007888", "about": { "@type": "MedicalCondition", "name": "Maladie de Leigh", "code": { "@type": "MedicalCode", "code": "D007888", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.520" } } }, { "@type": "MedicalWebPage", "name": "Myopathies mitochondriales", "alternateName": "Mitochondrial Myopathies", "url": "https://recherchemedicale.com/mesh/D017240", "about": { "@type": "MedicalCondition", "name": "Myopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017240", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Encéphalomyopathies mitochondriales", "alternateName": "Mitochondrial Encephalomyopathies", "url": "https://recherchemedicale.com/mesh/D017237", "about": { "@type": "MedicalCondition", "name": "Encéphalomyopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017237", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Encéphalomyopathies mitochondriales", "alternateName": "Mitochondrial Encephalomyopathies", "url": "https://recherchemedicale.com/mesh/D017237", "about": { "@type": "MedicalCondition", "name": "Encéphalomyopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017237", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en acyl CoA déshydrogénase", "alternateName": "Multiple Acyl Coenzyme A Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054069", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en acyl CoA déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.612" } } }, { "@type": "MedicalWebPage", "name": "Atrophie optique autosomique dominante", "alternateName": "Optic Atrophy, Autosomal Dominant", "url": "https://recherchemedicale.com/mesh/D029241", "about": { "@type": "MedicalCondition", "name": "Atrophie optique autosomique dominante", "code": { "@type": "MedicalCode", "code": "D029241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.665" } } }, { "@type": "MedicalWebPage", "name": "Atrophie optique héréditaire de Leber", "alternateName": "Optic Atrophy, Hereditary, Leber", "url": "https://recherchemedicale.com/mesh/D029242", "about": { "@type": "MedicalCondition", "name": "Atrophie optique héréditaire de Leber", "code": { "@type": "MedicalCode", "code": "D029242", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.670" } } }, { "@type": "MedicalWebPage", "name": "Déficit en pyruvate carboxylase", "alternateName": "Pyruvate Carboxylase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D015324", "about": { "@type": "MedicalCondition", "name": "Déficit en pyruvate carboxylase", "code": { "@type": "MedicalCode", "code": "D015324", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.705" } } }, { "@type": "MedicalWebPage", "name": "Déficit en complexe pyruvate-déshydrogénase", "alternateName": "Pyruvate Dehydrogenase Complex Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D015325", "about": { "@type": "MedicalCondition", "name": "Déficit en complexe pyruvate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D015325", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.710" } } } ] }, { "@type": "MedicalWebPage", "name": "Déficit en carbamoyl-phosphate synthase I", "alternateName": "Carbamoyl-Phosphate Synthase I Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D020165", "about": { "@type": "MedicalCondition", "name": "Déficit en carbamoyl-phosphate synthase I", "code": { "@type": "MedicalCode", "code": "D020165", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.097" } } }, { "@type": "MedicalWebPage", "name": "Déficit en cytochrome-c oxydase", "alternateName": "Cytochrome-c Oxidase Deficiency", "url": "https://recherchemedicale.com/mesh/D030401", "about": { "@type": "MedicalCondition", "name": "Déficit en cytochrome-c oxydase", "code": { "@type": "MedicalCode", "code": "D030401", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.195" } } }, { "@type": "MedicalWebPage", "name": "Ataxie de Friedreich", "alternateName": "Friedreich Ataxia", "url": "https://recherchemedicale.com/mesh/D005621", "about": { "@type": "MedicalCondition", "name": "Ataxie de Friedreich", "code": { "@type": "MedicalCode", "code": "D005621", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.300" } } }, { "@type": "MedicalWebPage", "name": "Maladie de Leigh", "alternateName": "Leigh Disease", "url": "https://recherchemedicale.com/mesh/D007888", "about": { "@type": "MedicalCondition", "name": "Maladie de Leigh", "code": { "@type": "MedicalCode", "code": "D007888", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.520" } } }, { "@type": "MedicalWebPage", "name": "Myopathies mitochondriales", "alternateName": "Mitochondrial Myopathies", "url": "https://recherchemedicale.com/mesh/D017240", "about": { "@type": "MedicalCondition", "name": "Myopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017240", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Encéphalomyopathies mitochondriales", "alternateName": "Mitochondrial Encephalomyopathies", "url": "https://recherchemedicale.com/mesh/D017237", "about": { "@type": "MedicalCondition", "name": "Encéphalomyopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017237", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Encéphalomyopathies mitochondriales", "alternateName": "Mitochondrial Encephalomyopathies", "url": "https://recherchemedicale.com/mesh/D017237", "about": { "@type": "MedicalCondition", "name": "Encéphalomyopathies mitochondriales", "code": { "@type": "MedicalCode", "code": "D017237", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome MELAS", "alternateName": "MELAS Syndrome", "url": "https://recherchemedicale.com/mesh/D017241", "about": { "@type": "MedicalCondition", "name": "Syndrome MELAS", "code": { "@type": "MedicalCode", "code": "D017241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.520" } } }, { "@type": "MedicalWebPage", "name": "Syndrome MERRF", "alternateName": "MERRF Syndrome", "url": "https://recherchemedicale.com/mesh/D017243", "about": { "@type": "MedicalCondition", "name": "Syndrome MERRF", "code": { "@type": "MedicalCode", "code": "D017243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.560.620.530" } } }, { "@type": "MedicalWebPage", "name": "Déficit multiple en acyl CoA déshydrogénase", "alternateName": "Multiple Acyl Coenzyme A Dehydrogenase Deficiency", "url": "https://recherchemedicale.com/mesh/D054069", "about": { "@type": "MedicalCondition", "name": "Déficit multiple en acyl CoA déshydrogénase", "code": { "@type": "MedicalCode", "code": "D054069", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.612" } } }, { "@type": "MedicalWebPage", "name": "Atrophie optique autosomique dominante", "alternateName": "Optic Atrophy, Autosomal Dominant", "url": "https://recherchemedicale.com/mesh/D029241", "about": { "@type": "MedicalCondition", "name": "Atrophie optique autosomique dominante", "code": { "@type": "MedicalCode", "code": "D029241", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.665" } } }, { "@type": "MedicalWebPage", "name": "Atrophie optique héréditaire de Leber", "alternateName": "Optic Atrophy, Hereditary, Leber", "url": "https://recherchemedicale.com/mesh/D029242", "about": { "@type": "MedicalCondition", "name": "Atrophie optique héréditaire de Leber", "code": { "@type": "MedicalCode", "code": "D029242", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.670" } } }, { "@type": "MedicalWebPage", "name": "Déficit en pyruvate carboxylase", "alternateName": "Pyruvate Carboxylase Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D015324", "about": { "@type": "MedicalCondition", "name": "Déficit en pyruvate carboxylase", "code": { "@type": "MedicalCode", "code": "D015324", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.705" } } }, { "@type": "MedicalWebPage", "name": "Déficit en complexe pyruvate-déshydrogénase", "alternateName": "Pyruvate Dehydrogenase Complex Deficiency Disease", "url": "https://recherchemedicale.com/mesh/D015325", "about": { "@type": "MedicalCondition", "name": "Déficit en complexe pyruvate-déshydrogénase", "code": { "@type": "MedicalCode", "code": "D015325", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.660.710" } } }, { "@type": "MedicalWebPage", "name": "Troubles du métabolisme du phosphore", "alternateName": "Phosphorus Metabolism Disorders", "url": "https://recherchemedicale.com/mesh/D010760", "about": { "@type": "MedicalCondition", "name": "Troubles du métabolisme du phosphore", "code": { "@type": "MedicalCode", "code": "D010760", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hyperphosphatémie", "alternateName": "Hyperphosphatemia", "url": "https://recherchemedicale.com/mesh/D054559", "about": { "@type": "MedicalCondition", "name": "Hyperphosphatémie", "code": { "@type": "MedicalCode", "code": "D054559", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.199" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatémie", "alternateName": "Hypophosphatemia", "url": "https://recherchemedicale.com/mesh/D017674", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie", "code": { "@type": "MedicalCode", "code": "D017674", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypophosphatémie familiale", "alternateName": "Hypophosphatemia, Familial", "url": "https://recherchemedicale.com/mesh/D007015", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie familiale", "code": { "@type": "MedicalCode", "code": "D007015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypophosphatémie familiale", "alternateName": "Hypophosphatemia, Familial", "url": "https://recherchemedicale.com/mesh/D007015", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie familiale", "code": { "@type": "MedicalCode", "code": "D007015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hyperphosphatémie", "alternateName": "Hyperphosphatemia", "url": "https://recherchemedicale.com/mesh/D054559", "about": { "@type": "MedicalCondition", "name": "Hyperphosphatémie", "code": { "@type": "MedicalCode", "code": "D054559", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.199" } } }, { "@type": "MedicalWebPage", "name": "Hypophosphatémie", "alternateName": "Hypophosphatemia", "url": "https://recherchemedicale.com/mesh/D017674", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie", "code": { "@type": "MedicalCode", "code": "D017674", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypophosphatémie familiale", "alternateName": "Hypophosphatemia, Familial", "url": "https://recherchemedicale.com/mesh/D007015", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie familiale", "code": { "@type": "MedicalCode", "code": "D007015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypophosphatémie familiale", "alternateName": "Hypophosphatemia, Familial", "url": "https://recherchemedicale.com/mesh/D007015", "about": { "@type": "MedicalCondition", "name": "Hypophosphatémie familiale", "code": { "@type": "MedicalCode", "code": "D007015", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.750.400.500" } } }, { "@type": "MedicalWebPage", "name": "Porphyries", "alternateName": "Porphyrias", "url": "https://recherchemedicale.com/mesh/D011164", "about": { "@type": "MedicalCondition", "name": "Porphyries", "code": { "@type": "MedicalCode", "code": "D011164", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Porphyrie érythropoïétique", "alternateName": "Porphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D017092", "about": { "@type": "MedicalCondition", "name": "Porphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D017092", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyries hépatiques", "alternateName": "Porphyrias, Hepatic", "url": "https://recherchemedicale.com/mesh/D017094", "about": { "@type": "MedicalCondition", "name": "Porphyries hépatiques", "code": { "@type": "MedicalCode", "code": "D017094", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Coproporphyrie héréditaire", "alternateName": "Coproporphyria, Hereditary", "url": "https://recherchemedicale.com/mesh/D046349", "about": { "@type": "MedicalCondition", "name": "Coproporphyrie héréditaire", "code": { "@type": "MedicalCode", "code": "D046349", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.074" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie aigüe intermittente", "alternateName": "Porphyria, Acute Intermittent", "url": "https://recherchemedicale.com/mesh/D017118", "about": { "@type": "MedicalCondition", "name": "Porphyrie aigüe intermittente", "code": { "@type": "MedicalCode", "code": "D017118", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.150" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie cutanée tardive", "alternateName": "Porphyria Cutanea Tarda", "url": "https://recherchemedicale.com/mesh/D017119", "about": { "@type": "MedicalCondition", "name": "Porphyrie cutanée tardive", "code": { "@type": "MedicalCode", "code": "D017119", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie hépatoérythropoïétique", "alternateName": "Porphyria, Hepatoerythropoietic", "url": "https://recherchemedicale.com/mesh/D017121", "about": { "@type": "MedicalCondition", "name": "Porphyrie hépatoérythropoïétique", "code": { "@type": "MedicalCode", "code": "D017121", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.437" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie variegata", "alternateName": "Porphyria, Variegate", "url": "https://recherchemedicale.com/mesh/D046350", "about": { "@type": "MedicalCondition", "name": "Porphyrie variegata", "code": { "@type": "MedicalCode", "code": "D046350", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.625" } } }, { "@type": "MedicalWebPage", "name": "Protoporphyrie érythropoïétique", "alternateName": "Protoporphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D046351", "about": { "@type": "MedicalCondition", "name": "Protoporphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D046351", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.812" } } } ] }, { "@type": "MedicalWebPage", "name": "Coproporphyrie héréditaire", "alternateName": "Coproporphyria, Hereditary", "url": "https://recherchemedicale.com/mesh/D046349", "about": { "@type": "MedicalCondition", "name": "Coproporphyrie héréditaire", "code": { "@type": "MedicalCode", "code": "D046349", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.074" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie aigüe intermittente", "alternateName": "Porphyria, Acute Intermittent", "url": "https://recherchemedicale.com/mesh/D017118", "about": { "@type": "MedicalCondition", "name": "Porphyrie aigüe intermittente", "code": { "@type": "MedicalCode", "code": "D017118", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.150" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie cutanée tardive", "alternateName": "Porphyria Cutanea Tarda", "url": "https://recherchemedicale.com/mesh/D017119", "about": { "@type": "MedicalCondition", "name": "Porphyrie cutanée tardive", "code": { "@type": "MedicalCode", "code": "D017119", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie hépatoérythropoïétique", "alternateName": "Porphyria, Hepatoerythropoietic", "url": "https://recherchemedicale.com/mesh/D017121", "about": { "@type": "MedicalCondition", "name": "Porphyrie hépatoérythropoïétique", "code": { "@type": "MedicalCode", "code": "D017121", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.437" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie variegata", "alternateName": "Porphyria, Variegate", "url": "https://recherchemedicale.com/mesh/D046350", "about": { "@type": "MedicalCondition", "name": "Porphyrie variegata", "code": { "@type": "MedicalCode", "code": "D046350", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.625" } } }, { "@type": "MedicalWebPage", "name": "Protoporphyrie érythropoïétique", "alternateName": "Protoporphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D046351", "about": { "@type": "MedicalCondition", "name": "Protoporphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D046351", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.812" } } } ] }, { "@type": "MedicalWebPage", "name": "Porphyrie érythropoïétique", "alternateName": "Porphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D017092", "about": { "@type": "MedicalCondition", "name": "Porphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D017092", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyries hépatiques", "alternateName": "Porphyrias, Hepatic", "url": "https://recherchemedicale.com/mesh/D017094", "about": { "@type": "MedicalCondition", "name": "Porphyries hépatiques", "code": { "@type": "MedicalCode", "code": "D017094", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Coproporphyrie héréditaire", "alternateName": "Coproporphyria, Hereditary", "url": "https://recherchemedicale.com/mesh/D046349", "about": { "@type": "MedicalCondition", "name": "Coproporphyrie héréditaire", "code": { "@type": "MedicalCode", "code": "D046349", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.074" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie aigüe intermittente", "alternateName": "Porphyria, Acute Intermittent", "url": "https://recherchemedicale.com/mesh/D017118", "about": { "@type": "MedicalCondition", "name": "Porphyrie aigüe intermittente", "code": { "@type": "MedicalCode", "code": "D017118", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.150" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie cutanée tardive", "alternateName": "Porphyria Cutanea Tarda", "url": "https://recherchemedicale.com/mesh/D017119", "about": { "@type": "MedicalCondition", "name": "Porphyrie cutanée tardive", "code": { "@type": "MedicalCode", "code": "D017119", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie hépatoérythropoïétique", "alternateName": "Porphyria, Hepatoerythropoietic", "url": "https://recherchemedicale.com/mesh/D017121", "about": { "@type": "MedicalCondition", "name": "Porphyrie hépatoérythropoïétique", "code": { "@type": "MedicalCode", "code": "D017121", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.437" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie variegata", "alternateName": "Porphyria, Variegate", "url": "https://recherchemedicale.com/mesh/D046350", "about": { "@type": "MedicalCondition", "name": "Porphyrie variegata", "code": { "@type": "MedicalCode", "code": "D046350", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.625" } } }, { "@type": "MedicalWebPage", "name": "Protoporphyrie érythropoïétique", "alternateName": "Protoporphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D046351", "about": { "@type": "MedicalCondition", "name": "Protoporphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D046351", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.812" } } } ] }, { "@type": "MedicalWebPage", "name": "Coproporphyrie héréditaire", "alternateName": "Coproporphyria, Hereditary", "url": "https://recherchemedicale.com/mesh/D046349", "about": { "@type": "MedicalCondition", "name": "Coproporphyrie héréditaire", "code": { "@type": "MedicalCode", "code": "D046349", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.074" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie aigüe intermittente", "alternateName": "Porphyria, Acute Intermittent", "url": "https://recherchemedicale.com/mesh/D017118", "about": { "@type": "MedicalCondition", "name": "Porphyrie aigüe intermittente", "code": { "@type": "MedicalCode", "code": "D017118", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.150" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie cutanée tardive", "alternateName": "Porphyria Cutanea Tarda", "url": "https://recherchemedicale.com/mesh/D017119", "about": { "@type": "MedicalCondition", "name": "Porphyrie cutanée tardive", "code": { "@type": "MedicalCode", "code": "D017119", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.250" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie hépatoérythropoïétique", "alternateName": "Porphyria, Hepatoerythropoietic", "url": "https://recherchemedicale.com/mesh/D017121", "about": { "@type": "MedicalCondition", "name": "Porphyrie hépatoérythropoïétique", "code": { "@type": "MedicalCode", "code": "D017121", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.437" } } }, { "@type": "MedicalWebPage", "name": "Porphyrie variegata", "alternateName": "Porphyria, Variegate", "url": "https://recherchemedicale.com/mesh/D046350", "about": { "@type": "MedicalCondition", "name": "Porphyrie variegata", "code": { "@type": "MedicalCode", "code": "D046350", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.625" } } }, { "@type": "MedicalWebPage", "name": "Protoporphyrie érythropoïétique", "alternateName": "Protoporphyria, Erythropoietic", "url": "https://recherchemedicale.com/mesh/D046351", "about": { "@type": "MedicalCondition", "name": "Protoporphyrie érythropoïétique", "code": { "@type": "MedicalCode", "code": "D046351", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.811.400.812" } } }, { "@type": "MedicalWebPage", "name": "Troubles de l'homéostasie des protéines", "alternateName": "Proteostasis Deficiencies", "url": "https://recherchemedicale.com/mesh/D057165", "about": { "@type": "MedicalCondition", "name": "Troubles de l'homéostasie des protéines", "code": { "@type": "MedicalCode", "code": "D057165", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Amyloïdose", "alternateName": "Amyloidosis", "url": "https://recherchemedicale.com/mesh/D000686", "about": { "@type": "MedicalCondition", "name": "Amyloïdose", "code": { "@type": "MedicalCode", "code": "D000686", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes", "alternateName": "Amyloid Neuropathies", "url": "https://recherchemedicale.com/mesh/D017772", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes", "code": { "@type": "MedicalCode", "code": "D017772", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.050" } } }, { "@type": "MedicalWebPage", "name": "Amyloïdose familiale", "alternateName": "Amyloidosis, Familial", "url": "https://recherchemedicale.com/mesh/D028226", "about": { "@type": "MedicalCondition", "name": "Amyloïdose familiale", "code": { "@type": "MedicalCode", "code": "D028226", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale", "alternateName": "Cerebral Amyloid Angiopathy", "url": "https://recherchemedicale.com/mesh/D016657", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale", "code": { "@type": "MedicalCode", "code": "D016657", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes", "alternateName": "Amyloid Neuropathies", "url": "https://recherchemedicale.com/mesh/D017772", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes", "code": { "@type": "MedicalCode", "code": "D017772", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.050" } } }, { "@type": "MedicalWebPage", "name": "Amyloïdose familiale", "alternateName": "Amyloidosis, Familial", "url": "https://recherchemedicale.com/mesh/D028226", "about": { "@type": "MedicalCondition", "name": "Amyloïdose familiale", "code": { "@type": "MedicalCode", "code": "D028226", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale", "alternateName": "Cerebral Amyloid Angiopathy", "url": "https://recherchemedicale.com/mesh/D016657", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale", "code": { "@type": "MedicalCode", "code": "D016657", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } }, { "@type": "MedicalWebPage", "name": "Synucléinopathies", "alternateName": "Synucleinopathies", "url": "https://recherchemedicale.com/mesh/D000080874", "about": { "@type": "MedicalCondition", "name": "Synucléinopathies", "code": { "@type": "MedicalCode", "code": "D000080874", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.650" } } }, { "@type": "MedicalWebPage", "name": "Protéinopathies TDP-43", "alternateName": "TDP-43 Proteinopathies", "url": "https://recherchemedicale.com/mesh/D057177", "about": { "@type": "MedicalCondition", "name": "Protéinopathies TDP-43", "code": { "@type": "MedicalCode", "code": "D057177", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose latérale amyotrophique", "alternateName": "Amyotrophic Lateral Sclerosis", "url": "https://recherchemedicale.com/mesh/D000690", "about": { "@type": "MedicalCondition", "name": "Sclérose latérale amyotrophique", "code": { "@type": "MedicalCode", "code": "D000690", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose latérale amyotrophique", "alternateName": "Amyotrophic Lateral Sclerosis", "url": "https://recherchemedicale.com/mesh/D000690", "about": { "@type": "MedicalCondition", "name": "Sclérose latérale amyotrophique", "code": { "@type": "MedicalCode", "code": "D000690", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Amyloïdose", "alternateName": "Amyloidosis", "url": "https://recherchemedicale.com/mesh/D000686", "about": { "@type": "MedicalCondition", "name": "Amyloïdose", "code": { "@type": "MedicalCode", "code": "D000686", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes", "alternateName": "Amyloid Neuropathies", "url": "https://recherchemedicale.com/mesh/D017772", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes", "code": { "@type": "MedicalCode", "code": "D017772", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.050" } } }, { "@type": "MedicalWebPage", "name": "Amyloïdose familiale", "alternateName": "Amyloidosis, Familial", "url": "https://recherchemedicale.com/mesh/D028226", "about": { "@type": "MedicalCondition", "name": "Amyloïdose familiale", "code": { "@type": "MedicalCode", "code": "D028226", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale", "alternateName": "Cerebral Amyloid Angiopathy", "url": "https://recherchemedicale.com/mesh/D016657", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale", "code": { "@type": "MedicalCode", "code": "D016657", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes", "alternateName": "Amyloid Neuropathies", "url": "https://recherchemedicale.com/mesh/D017772", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes", "code": { "@type": "MedicalCode", "code": "D017772", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.050" } } }, { "@type": "MedicalWebPage", "name": "Amyloïdose familiale", "alternateName": "Amyloidosis, Familial", "url": "https://recherchemedicale.com/mesh/D028226", "about": { "@type": "MedicalCondition", "name": "Amyloïdose familiale", "code": { "@type": "MedicalCode", "code": "D028226", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Neuropathies amyloïdes familiales", "alternateName": "Amyloid Neuropathies, Familial", "url": "https://recherchemedicale.com/mesh/D028227", "about": { "@type": "MedicalCondition", "name": "Neuropathies amyloïdes familiales", "code": { "@type": "MedicalCode", "code": "D028227", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.075.050" } } }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale", "alternateName": "Cerebral Amyloid Angiopathy", "url": "https://recherchemedicale.com/mesh/D016657", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale", "code": { "@type": "MedicalCode", "code": "D016657", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } } ] }, { "@type": "MedicalWebPage", "name": "Angiopathie amyloïde cérébrale familiale", "alternateName": "Cerebral Amyloid Angiopathy, Familial", "url": "https://recherchemedicale.com/mesh/D028243", "about": { "@type": "MedicalCondition", "name": "Angiopathie amyloïde cérébrale familiale", "code": { "@type": "MedicalCode", "code": "D028243", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.500.100.160" } } }, { "@type": "MedicalWebPage", "name": "Synucléinopathies", "alternateName": "Synucleinopathies", "url": "https://recherchemedicale.com/mesh/D000080874", "about": { "@type": "MedicalCondition", "name": "Synucléinopathies", "code": { "@type": "MedicalCode", "code": "D000080874", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.650" } } }, { "@type": "MedicalWebPage", "name": "Protéinopathies TDP-43", "alternateName": "TDP-43 Proteinopathies", "url": "https://recherchemedicale.com/mesh/D057177", "about": { "@type": "MedicalCondition", "name": "Protéinopathies TDP-43", "code": { "@type": "MedicalCode", "code": "D057177", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Sclérose latérale amyotrophique", "alternateName": "Amyotrophic Lateral Sclerosis", "url": "https://recherchemedicale.com/mesh/D000690", "about": { "@type": "MedicalCondition", "name": "Sclérose latérale amyotrophique", "code": { "@type": "MedicalCode", "code": "D000690", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800.050" } } } ] }, { "@type": "MedicalWebPage", "name": "Sclérose latérale amyotrophique", "alternateName": "Amyotrophic Lateral Sclerosis", "url": "https://recherchemedicale.com/mesh/D000690", "about": { "@type": "MedicalCondition", "name": "Sclérose latérale amyotrophique", "code": { "@type": "MedicalCode", "code": "D000690", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.845.800.050" } } }, { "@type": "MedicalWebPage", "name": "Dermatoses métaboliques", "alternateName": "Skin Diseases, Metabolic", "url": "https://recherchemedicale.com/mesh/D012875", "about": { "@type": "MedicalCondition", "name": "Dermatoses métaboliques", "code": { "@type": "MedicalCode", "code": "D012875", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Lipodystrophie", "alternateName": "Lipodystrophy", "url": "https://recherchemedicale.com/mesh/D008060", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie", "code": { "@type": "MedicalCode", "code": "D008060", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Lipodystrophie généralisée congénitale", "alternateName": "Lipodystrophy, Congenital Generalized", "url": "https://recherchemedicale.com/mesh/D052497", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie généralisée congénitale", "code": { "@type": "MedicalCode", "code": "D052497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.550" } } }, { "@type": "MedicalWebPage", "name": "Lipodystrophie partielle familiale", "alternateName": "Lipodystrophy, Familial Partial", "url": "https://recherchemedicale.com/mesh/D052496", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie partielle familiale", "code": { "@type": "MedicalCode", "code": "D052496", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.700" } } } ] }, { "@type": "MedicalWebPage", "name": "Lipodystrophie généralisée congénitale", "alternateName": "Lipodystrophy, Congenital Generalized", "url": "https://recherchemedicale.com/mesh/D052497", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie généralisée congénitale", "code": { "@type": "MedicalCode", "code": "D052497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.550" } } }, { "@type": "MedicalWebPage", "name": "Lipodystrophie partielle familiale", "alternateName": "Lipodystrophy, Familial Partial", "url": "https://recherchemedicale.com/mesh/D052496", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie partielle familiale", "code": { "@type": "MedicalCode", "code": "D052496", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.700" } } }, { "@type": "MedicalWebPage", "name": "Nécrobiose lipoïdique", "alternateName": "Necrobiosis Lipoidica", "url": "https://recherchemedicale.com/mesh/D009335", "about": { "@type": "MedicalCondition", "name": "Nécrobiose lipoïdique", "code": { "@type": "MedicalCode", "code": "D009335", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.495" } } } ] }, { "@type": "MedicalWebPage", "name": "Lipodystrophie", "alternateName": "Lipodystrophy", "url": "https://recherchemedicale.com/mesh/D008060", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie", "code": { "@type": "MedicalCode", "code": "D008060", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Lipodystrophie généralisée congénitale", "alternateName": "Lipodystrophy, Congenital Generalized", "url": "https://recherchemedicale.com/mesh/D052497", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie généralisée congénitale", "code": { "@type": "MedicalCode", "code": "D052497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.550" } } }, { "@type": "MedicalWebPage", "name": "Lipodystrophie partielle familiale", "alternateName": "Lipodystrophy, Familial Partial", "url": "https://recherchemedicale.com/mesh/D052496", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie partielle familiale", "code": { "@type": "MedicalCode", "code": "D052496", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.700" } } } ] }, { "@type": "MedicalWebPage", "name": "Lipodystrophie généralisée congénitale", "alternateName": "Lipodystrophy, Congenital Generalized", "url": "https://recherchemedicale.com/mesh/D052497", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie généralisée congénitale", "code": { "@type": "MedicalCode", "code": "D052497", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.550" } } }, { "@type": "MedicalWebPage", "name": "Lipodystrophie partielle familiale", "alternateName": "Lipodystrophy, Familial Partial", "url": "https://recherchemedicale.com/mesh/D052496", "about": { "@type": "MedicalCondition", "name": "Lipodystrophie partielle familiale", "code": { "@type": "MedicalCode", "code": "D052496", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.391.700" } } }, { "@type": "MedicalWebPage", "name": "Nécrobiose lipoïdique", "alternateName": "Necrobiosis Lipoidica", "url": "https://recherchemedicale.com/mesh/D009335", "about": { "@type": "MedicalCondition", "name": "Nécrobiose lipoïdique", "code": { "@type": "MedicalCode", "code": "D009335", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.880.495" } } }, { "@type": "MedicalWebPage", "name": "Troubles de l'équilibre hydroélectrolytique", "alternateName": "Water-Electrolyte Imbalance", "url": "https://recherchemedicale.com/mesh/D014883", "about": { "@type": "MedicalCondition", "name": "Troubles de l'équilibre hydroélectrolytique", "code": { "@type": "MedicalCode", "code": "D014883", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Hypercalcémie", "alternateName": "Hypercalcemia", "url": "https://recherchemedicale.com/mesh/D006934", "about": { "@type": "MedicalCondition", "name": "Hypercalcémie", "code": { "@type": "MedicalCode", "code": "D006934", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.340" } } }, { "@type": "MedicalWebPage", "name": "Hyperkaliémie", "alternateName": "Hyperkalemia", "url": "https://recherchemedicale.com/mesh/D006947", "about": { "@type": "MedicalCondition", "name": "Hyperkaliémie", "code": { "@type": "MedicalCode", "code": "D006947", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.396" } } }, { "@type": "MedicalWebPage", "name": "Hypernatrémie", "alternateName": "Hypernatremia", "url": "https://recherchemedicale.com/mesh/D006955", "about": { "@type": "MedicalCondition", "name": "Hypernatrémie", "code": { "@type": "MedicalCode", "code": "D006955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.452" } } }, { "@type": "MedicalWebPage", "name": "Hypocalcémie", "alternateName": "Hypocalcemia", "url": "https://recherchemedicale.com/mesh/D006996", "about": { "@type": "MedicalCondition", "name": "Hypocalcémie", "code": { "@type": "MedicalCode", "code": "D006996", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.509" } } }, { "@type": "MedicalWebPage", "name": "Hypokaliémie", "alternateName": "Hypokalemia", "url": "https://recherchemedicale.com/mesh/D007008", "about": { "@type": "MedicalCondition", "name": "Hypokaliémie", "code": { "@type": "MedicalCode", "code": "D007008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.565" } } }, { "@type": "MedicalWebPage", "name": "Hyponatrémie", "alternateName": "Hyponatremia", "url": "https://recherchemedicale.com/mesh/D007010", "about": { "@type": "MedicalCondition", "name": "Hyponatrémie", "code": { "@type": "MedicalCode", "code": "D007010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Hypercalcémie", "alternateName": "Hypercalcemia", "url": "https://recherchemedicale.com/mesh/D006934", "about": { "@type": "MedicalCondition", "name": "Hypercalcémie", "code": { "@type": "MedicalCode", "code": "D006934", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.340" } } }, { "@type": "MedicalWebPage", "name": "Hyperkaliémie", "alternateName": "Hyperkalemia", "url": "https://recherchemedicale.com/mesh/D006947", "about": { "@type": "MedicalCondition", "name": "Hyperkaliémie", "code": { "@type": "MedicalCode", "code": "D006947", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.396" } } }, { "@type": "MedicalWebPage", "name": "Hypernatrémie", "alternateName": "Hypernatremia", "url": "https://recherchemedicale.com/mesh/D006955", "about": { "@type": "MedicalCondition", "name": "Hypernatrémie", "code": { "@type": "MedicalCode", "code": "D006955", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.452" } } }, { "@type": "MedicalWebPage", "name": "Hypocalcémie", "alternateName": "Hypocalcemia", "url": "https://recherchemedicale.com/mesh/D006996", "about": { "@type": "MedicalCondition", "name": "Hypocalcémie", "code": { "@type": "MedicalCode", "code": "D006996", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.509" } } }, { "@type": "MedicalWebPage", "name": "Hypokaliémie", "alternateName": "Hypokalemia", "url": "https://recherchemedicale.com/mesh/D007008", "about": { "@type": "MedicalCondition", "name": "Hypokaliémie", "code": { "@type": "MedicalCode", "code": "D007008", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.565" } } }, { "@type": "MedicalWebPage", "name": "Hyponatrémie", "alternateName": "Hyponatremia", "url": "https://recherchemedicale.com/mesh/D007010", "about": { "@type": "MedicalCondition", "name": "Hyponatrémie", "code": { "@type": "MedicalCode", "code": "D007010", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.452.950.620" } } } ] }, { "@type": "MedicalWebPage", "name": "Troubles nutritionnels", "alternateName": "Nutrition Disorders", "url": "https://recherchemedicale.com/mesh/D009748", "about": { "@type": "MedicalCondition", "name": "Troubles nutritionnels", "code": { "@type": "MedicalCode", "code": "D009748", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Troubles nutritionnels de l'enfant", "alternateName": "Child Nutrition Disorders", "url": "https://recherchemedicale.com/mesh/D015362", "about": { "@type": "MedicalCondition", "name": "Troubles nutritionnels de l'enfant", "code": { "@type": "MedicalCode", "code": "D015362", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.180" } } }, { "@type": "MedicalWebPage", "name": "Hypervitaminose A", "alternateName": "Hypervitaminosis A", "url": "https://recherchemedicale.com/mesh/D006986", "about": { "@type": "MedicalCondition", "name": "Hypervitaminose A", "code": { "@type": "MedicalCode", "code": "D006986", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.301" } } }, { "@type": "MedicalWebPage", "name": "Troubles nutritionnels du nourrisson", "alternateName": "Infant Nutrition Disorders", "url": "https://recherchemedicale.com/mesh/D007228", "about": { "@type": "MedicalCondition", "name": "Troubles nutritionnels du nourrisson", "code": { "@type": "MedicalCode", "code": "D007228", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.422" } } }, { "@type": "MedicalWebPage", "name": "Malnutrition", "alternateName": "Malnutrition", "url": "https://recherchemedicale.com/mesh/D044342", "about": { "@type": "MedicalCondition", "name": "Malnutrition", "code": { "@type": "MedicalCode", "code": "D044342", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Maladies de carence", "alternateName": "Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D003677", "about": { "@type": "MedicalCondition", "name": "Maladies de carence", "code": { "@type": "MedicalCode", "code": "D003677", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Avitaminoses", "alternateName": "Avitaminosis", "url": "https://recherchemedicale.com/mesh/D001361", "about": { "@type": "MedicalCondition", "name": "Avitaminoses", "code": { "@type": "MedicalCode", "code": "D001361", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } }, { "@type": "MedicalWebPage", "name": "Magnésium, carence", "alternateName": "Magnesium Deficiency", "url": "https://recherchemedicale.com/mesh/D008275", "about": { "@type": "MedicalCondition", "name": "Magnésium, carence", "code": { "@type": "MedicalCode", "code": "D008275", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.439" } } }, { "@type": "MedicalWebPage", "name": "Potassium, carence", "alternateName": "Potassium Deficiency", "url": "https://recherchemedicale.com/mesh/D011191", "about": { "@type": "MedicalCondition", "name": "Potassium, carence", "code": { "@type": "MedicalCode", "code": "D011191", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.617" } } }, { "@type": "MedicalWebPage", "name": "Carence protéique", "alternateName": "Protein Deficiency", "url": "https://recherchemedicale.com/mesh/D011488", "about": { "@type": "MedicalCondition", "name": "Carence protéique", "code": { "@type": "MedicalCode", "code": "D011488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Avitaminoses", "alternateName": "Avitaminosis", "url": "https://recherchemedicale.com/mesh/D001361", "about": { "@type": "MedicalCondition", "name": "Avitaminoses", "code": { "@type": "MedicalCode", "code": "D001361", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } }, { "@type": "MedicalWebPage", "name": "Magnésium, carence", "alternateName": "Magnesium Deficiency", "url": "https://recherchemedicale.com/mesh/D008275", "about": { "@type": "MedicalCondition", "name": "Magnésium, carence", "code": { "@type": "MedicalCode", "code": "D008275", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.439" } } }, { "@type": "MedicalWebPage", "name": "Potassium, carence", "alternateName": "Potassium Deficiency", "url": "https://recherchemedicale.com/mesh/D011191", "about": { "@type": "MedicalCondition", "name": "Potassium, carence", "code": { "@type": "MedicalCode", "code": "D011191", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.617" } } }, { "@type": "MedicalWebPage", "name": "Carence protéique", "alternateName": "Protein Deficiency", "url": "https://recherchemedicale.com/mesh/D011488", "about": { "@type": "MedicalCondition", "name": "Carence protéique", "code": { "@type": "MedicalCode", "code": "D011488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } }, { "@type": "MedicalWebPage", "name": "Troubles nutritionnels du foetus", "alternateName": "Fetal Nutrition Disorders", "url": "https://recherchemedicale.com/mesh/D048070", "about": { "@type": "MedicalCondition", "name": "Troubles nutritionnels du foetus", "code": { "@type": "MedicalCode", "code": "D048070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.625" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de renutrition", "alternateName": "Refeeding Syndrome", "url": "https://recherchemedicale.com/mesh/D055677", "about": { "@type": "MedicalCondition", "name": "Syndrome de renutrition", "code": { "@type": "MedicalCode", "code": "D055677", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.687" } } }, { "@type": "MedicalWebPage", "name": "Malnutrition aigüe sévère", "alternateName": "Severe Acute Malnutrition", "url": "https://recherchemedicale.com/mesh/D000067011", "about": { "@type": "MedicalCondition", "name": "Malnutrition aigüe sévère", "code": { "@type": "MedicalCode", "code": "D000067011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Kwashiorkor", "alternateName": "Kwashiorkor", "url": "https://recherchemedicale.com/mesh/D007732", "about": { "@type": "MedicalCondition", "name": "Kwashiorkor", "code": { "@type": "MedicalCode", "code": "D007732", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Kwashiorkor", "alternateName": "Kwashiorkor", "url": "https://recherchemedicale.com/mesh/D007732", "about": { "@type": "MedicalCondition", "name": "Kwashiorkor", "code": { "@type": "MedicalCode", "code": "D007732", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719.500" } } }, { "@type": "MedicalWebPage", "name": "Inanition", "alternateName": "Starvation", "url": "https://recherchemedicale.com/mesh/D013217", "about": { "@type": "MedicalCondition", "name": "Inanition", "code": { "@type": "MedicalCode", "code": "D013217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.750" } } } ] }, { "@type": "MedicalWebPage", "name": "Maladies de carence", "alternateName": "Deficiency Diseases", "url": "https://recherchemedicale.com/mesh/D003677", "about": { "@type": "MedicalCondition", "name": "Maladies de carence", "code": { "@type": "MedicalCode", "code": "D003677", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Avitaminoses", "alternateName": "Avitaminosis", "url": "https://recherchemedicale.com/mesh/D001361", "about": { "@type": "MedicalCondition", "name": "Avitaminoses", "code": { "@type": "MedicalCode", "code": "D001361", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } }, { "@type": "MedicalWebPage", "name": "Magnésium, carence", "alternateName": "Magnesium Deficiency", "url": "https://recherchemedicale.com/mesh/D008275", "about": { "@type": "MedicalCondition", "name": "Magnésium, carence", "code": { "@type": "MedicalCode", "code": "D008275", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.439" } } }, { "@type": "MedicalWebPage", "name": "Potassium, carence", "alternateName": "Potassium Deficiency", "url": "https://recherchemedicale.com/mesh/D011191", "about": { "@type": "MedicalCondition", "name": "Potassium, carence", "code": { "@type": "MedicalCode", "code": "D011191", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.617" } } }, { "@type": "MedicalWebPage", "name": "Carence protéique", "alternateName": "Protein Deficiency", "url": "https://recherchemedicale.com/mesh/D011488", "about": { "@type": "MedicalCondition", "name": "Carence protéique", "code": { "@type": "MedicalCode", "code": "D011488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Avitaminoses", "alternateName": "Avitaminosis", "url": "https://recherchemedicale.com/mesh/D001361", "about": { "@type": "MedicalCondition", "name": "Avitaminoses", "code": { "@type": "MedicalCode", "code": "D001361", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en acide ascorbique", "alternateName": "Ascorbic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D001206", "about": { "@type": "MedicalCondition", "name": "Carence en acide ascorbique", "code": { "@type": "MedicalCode", "code": "D001206", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } } ] }, { "@type": "MedicalWebPage", "name": "Scorbut", "alternateName": "Scurvy", "url": "https://recherchemedicale.com/mesh/D012614", "about": { "@type": "MedicalCondition", "name": "Scorbut", "code": { "@type": "MedicalCode", "code": "D012614", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.115.661" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine A", "alternateName": "Vitamin A Deficiency", "url": "https://recherchemedicale.com/mesh/D014802", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine A", "code": { "@type": "MedicalCode", "code": "D014802", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.628" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamines B", "alternateName": "Vitamin B Deficiency", "url": "https://recherchemedicale.com/mesh/D014804", "about": { "@type": "MedicalCondition", "name": "Carence en vitamines B", "code": { "@type": "MedicalCode", "code": "D014804", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Carence en choline", "alternateName": "Choline Deficiency", "url": "https://recherchemedicale.com/mesh/D002796", "about": { "@type": "MedicalCondition", "name": "Carence en choline", "code": { "@type": "MedicalCode", "code": "D002796", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.160" } } }, { "@type": "MedicalWebPage", "name": "Carence en acide folique", "alternateName": "Folic Acid Deficiency", "url": "https://recherchemedicale.com/mesh/D005494", "about": { "@type": "MedicalCondition", "name": "Carence en acide folique", "code": { "@type": "MedicalCode", "code": "D005494", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.308" } } }, { "@type": "MedicalWebPage", "name": "Hyperhomocystéinémie", "alternateName": "Hyperhomocysteinemia", "url": "https://recherchemedicale.com/mesh/D020138", "about": { "@type": "MedicalCondition", "name": "Hyperhomocystéinémie", "code": { "@type": "MedicalCode", "code": "D020138", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.418" } } }, { "@type": "MedicalWebPage", "name": "Pellagre", "alternateName": "Pellagra", "url": "https://recherchemedicale.com/mesh/D010383", "about": { "@type": "MedicalCondition", "name": "Pellagre", "code": { "@type": "MedicalCode", "code": "D010383", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.529" } } }, { "@type": "MedicalWebPage", "name": "Carence en riboflavine", "alternateName": "Riboflavin Deficiency", "url": "https://recherchemedicale.com/mesh/D012257", "about": { "@type": "MedicalCondition", "name": "Carence en riboflavine", "code": { "@type": "MedicalCode", "code": "D012257", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.713" } } }, { "@type": "MedicalWebPage", "name": "Carence en thiamine", "alternateName": "Thiamine Deficiency", "url": "https://recherchemedicale.com/mesh/D013832", "about": { "@type": "MedicalCondition", "name": "Carence en thiamine", "code": { "@type": "MedicalCode", "code": "D013832", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } } ] }, { "@type": "MedicalWebPage", "name": "Béribéri", "alternateName": "Beriberi", "url": "https://recherchemedicale.com/mesh/D001602", "about": { "@type": "MedicalCondition", "name": "Béribéri", "code": { "@type": "MedicalCode", "code": "D001602", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.827.223" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B6", "alternateName": "Vitamin B 6 Deficiency", "url": "https://recherchemedicale.com/mesh/D026681", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B6", "code": { "@type": "MedicalCode", "code": "D026681", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.901" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine B12", "alternateName": "Vitamin B 12 Deficiency", "url": "https://recherchemedicale.com/mesh/D014806", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine B12", "code": { "@type": "MedicalCode", "code": "D014806", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } } ] }, { "@type": "MedicalWebPage", "name": "Anémie pernicieuse", "alternateName": "Anemia, Pernicious", "url": "https://recherchemedicale.com/mesh/D000752", "about": { "@type": "MedicalCondition", "name": "Anémie pernicieuse", "code": { "@type": "MedicalCode", "code": "D000752", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.699.923.280" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine D", "alternateName": "Vitamin D Deficiency", "url": "https://recherchemedicale.com/mesh/D014808", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine D", "code": { "@type": "MedicalCode", "code": "D014808", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme", "alternateName": "Rickets", "url": "https://recherchemedicale.com/mesh/D012279", "about": { "@type": "MedicalCondition", "name": "Rachitisme", "code": { "@type": "MedicalCode", "code": "D012279", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Ostéomalacie", "alternateName": "Osteomalacia", "url": "https://recherchemedicale.com/mesh/D010018", "about": { "@type": "MedicalCondition", "name": "Ostéomalacie", "code": { "@type": "MedicalCode", "code": "D010018", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.640" } } }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique", "alternateName": "Rickets, Hypophosphatemic", "url": "https://recherchemedicale.com/mesh/D063730", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique", "code": { "@type": "MedicalCode", "code": "D063730", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Rachitisme hypophosphatémique familial", "alternateName": "Familial Hypophosphatemic Rickets", "url": "https://recherchemedicale.com/mesh/D053098", "about": { "@type": "MedicalCondition", "name": "Rachitisme hypophosphatémique familial", "code": { "@type": "MedicalCode", "code": "D053098", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.770.734.875.500" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine E", "alternateName": "Vitamin E Deficiency", "url": "https://recherchemedicale.com/mesh/D014811", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine E", "code": { "@type": "MedicalCode", "code": "D014811", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.841" } } }, { "@type": "MedicalWebPage", "name": "Carence en vitamine K", "alternateName": "Vitamin K Deficiency", "url": "https://recherchemedicale.com/mesh/D014813", "about": { "@type": "MedicalCondition", "name": "Carence en vitamine K", "code": { "@type": "MedicalCode", "code": "D014813", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } } ] }, { "@type": "MedicalWebPage", "name": "Saignement dû au déficit en vitamine K", "alternateName": "Vitamin K Deficiency Bleeding", "url": "https://recherchemedicale.com/mesh/D006475", "about": { "@type": "MedicalCondition", "name": "Saignement dû au déficit en vitamine K", "code": { "@type": "MedicalCode", "code": "D006475", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.133.912.360" } } }, { "@type": "MedicalWebPage", "name": "Magnésium, carence", "alternateName": "Magnesium Deficiency", "url": "https://recherchemedicale.com/mesh/D008275", "about": { "@type": "MedicalCondition", "name": "Magnésium, carence", "code": { "@type": "MedicalCode", "code": "D008275", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.439" } } }, { "@type": "MedicalWebPage", "name": "Potassium, carence", "alternateName": "Potassium Deficiency", "url": "https://recherchemedicale.com/mesh/D011191", "about": { "@type": "MedicalCondition", "name": "Potassium, carence", "code": { "@type": "MedicalCode", "code": "D011191", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.617" } } }, { "@type": "MedicalWebPage", "name": "Carence protéique", "alternateName": "Protein Deficiency", "url": "https://recherchemedicale.com/mesh/D011488", "about": { "@type": "MedicalCondition", "name": "Carence protéique", "code": { "@type": "MedicalCode", "code": "D011488", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } } ] }, { "@type": "MedicalWebPage", "name": "Malnutrition protéinocalorique", "alternateName": "Protein-Energy Malnutrition", "url": "https://recherchemedicale.com/mesh/D011502", "about": { "@type": "MedicalCondition", "name": "Malnutrition protéinocalorique", "code": { "@type": "MedicalCode", "code": "D011502", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.500.708.626" } } }, { "@type": "MedicalWebPage", "name": "Troubles nutritionnels du foetus", "alternateName": "Fetal Nutrition Disorders", "url": "https://recherchemedicale.com/mesh/D048070", "about": { "@type": "MedicalCondition", "name": "Troubles nutritionnels du foetus", "code": { "@type": "MedicalCode", "code": "D048070", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.625" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de renutrition", "alternateName": "Refeeding Syndrome", "url": "https://recherchemedicale.com/mesh/D055677", "about": { "@type": "MedicalCondition", "name": "Syndrome de renutrition", "code": { "@type": "MedicalCode", "code": "D055677", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.687" } } }, { "@type": "MedicalWebPage", "name": "Malnutrition aigüe sévère", "alternateName": "Severe Acute Malnutrition", "url": "https://recherchemedicale.com/mesh/D000067011", "about": { "@type": "MedicalCondition", "name": "Malnutrition aigüe sévère", "code": { "@type": "MedicalCode", "code": "D000067011", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Kwashiorkor", "alternateName": "Kwashiorkor", "url": "https://recherchemedicale.com/mesh/D007732", "about": { "@type": "MedicalCondition", "name": "Kwashiorkor", "code": { "@type": "MedicalCode", "code": "D007732", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719.500" } } } ] }, { "@type": "MedicalWebPage", "name": "Kwashiorkor", "alternateName": "Kwashiorkor", "url": "https://recherchemedicale.com/mesh/D007732", "about": { "@type": "MedicalCondition", "name": "Kwashiorkor", "code": { "@type": "MedicalCode", "code": "D007732", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.719.500" } } }, { "@type": "MedicalWebPage", "name": "Inanition", "alternateName": "Starvation", "url": "https://recherchemedicale.com/mesh/D013217", "about": { "@type": "MedicalCondition", "name": "Inanition", "code": { "@type": "MedicalCode", "code": "D013217", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.521.750" } } }, { "@type": "MedicalWebPage", "name": "Surnutrition", "alternateName": "Overnutrition", "url": "https://recherchemedicale.com/mesh/D044343", "about": { "@type": "MedicalCondition", "name": "Surnutrition", "code": { "@type": "MedicalCode", "code": "D044343", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.726" } }, "hasPart": [ { "@type": "MedicalWebPage", "name": "Syndrome obésité hypoventilation", "alternateName": "Obesity Hypoventilation Syndrome", "url": "https://recherchemedicale.com/mesh/D010845", "about": { "@type": "MedicalCondition", "name": "Syndrome obésité hypoventilation", "code": { "@type": "MedicalCode", "code": "D010845", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.726.750.500.600" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Prader-Willi", "alternateName": "Prader-Willi Syndrome", "url": "https://recherchemedicale.com/mesh/D011218", "about": { "@type": "MedicalCondition", "name": "Syndrome de Prader-Willi", "code": { "@type": "MedicalCode", "code": "D011218", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.726.750.500.740" } } } ] }, { "@type": "MedicalWebPage", "name": "Syndrome obésité hypoventilation", "alternateName": "Obesity Hypoventilation Syndrome", "url": "https://recherchemedicale.com/mesh/D010845", "about": { "@type": "MedicalCondition", "name": "Syndrome obésité hypoventilation", "code": { "@type": "MedicalCode", "code": "D010845", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.726.750.500.600" } } }, { "@type": "MedicalWebPage", "name": "Syndrome de Prader-Willi", "alternateName": "Prader-Willi Syndrome", "url": "https://recherchemedicale.com/mesh/D011218", "about": { "@type": "MedicalCondition", "name": "Syndrome de Prader-Willi", "code": { "@type": "MedicalCode", "code": "D011218", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.726.750.500.740" } } }, { "@type": "MedicalWebPage", "name": "Syndrome cachectique", "alternateName": "Wasting Syndrome", "url": "https://recherchemedicale.com/mesh/D019282", "about": { "@type": "MedicalCondition", "name": "Syndrome cachectique", "code": { "@type": "MedicalCode", "code": "D019282", "codingSystem": "MeSH" }, "identifier": { "@type": "PropertyValue", "propertyID": "MeSH Tree", "value": "C18.654.940" } } } ] } ], "about": { "@type": "MedicalCondition", "name": "Maladies métaboliques et nutritionnelles", "alternateName": "Nutritional and Metabolic Diseases", "code": { "@type": "MedicalCode", "code": "D009750", "codingSystem": "MeSH" } }, "author": [ { "@type": "Person", "name": "Guoyao Wu", "url": "https://recherchemedicale.com/author/Guoyao%20Wu", "affiliation": { "@type": "Organization", "name": "Department of Animal Science, Texas A&M University, College Station, TX, 77843, USA. g-wu@tamu.edu." } }, { "@type": "Person", "name": "Annabel Biruete", "url": "https://recherchemedicale.com/author/Annabel%20Biruete", "affiliation": { "@type": "Organization", "name": "Department of Nutrition Science, Purdue University, West Lafayette, Indiana, USA, Division of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana." } }, { "@type": "Person", "name": "Angela Yee-Moon Wang", "url": "https://recherchemedicale.com/author/Angela%20Yee-Moon%20Wang", "affiliation": { "@type": "Organization", "name": "Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China." } }, { "@type": "Person", "name": "Omar Ramos-Lopez", "url": "https://recherchemedicale.com/author/Omar%20Ramos-Lopez", "affiliation": { "@type": "Organization", "name": "Medicine and Psychology School, Autonomous University of Baja California, Tijuana, Baja California, Mexico." } }, { "@type": "Person", "name": "Shlomit Shalitin", "url": "https://recherchemedicale.com/author/Shlomit%20Shalitin", "affiliation": { "@type": "Organization", "name": "" } } ], "citation": [ { "@type": "ScholarlyArticle", "name": "Vitamin B12 in Cats: Nutrition, Metabolism, and Disease.", "datePublished": "2023-04-26", "url": "https://recherchemedicale.com/article/37174511", "identifier": { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.3390/ani13091474" } }, { "@type": "ScholarlyArticle", "name": "Metabolic Research in Aquatic Animal Nutrition, Physiology and Disease.", "datePublished": "2023-12-28", "url": "https://recherchemedicale.com/article/38248825", "identifier": { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.3390/metabo14010022" } }, { "@type": "ScholarlyArticle", "name": "Nutritional Status and Metabolism in Celiac Disease: Narrative Review.", "datePublished": "2023-08-03", "url": "https://recherchemedicale.com/article/37568509", "identifier": { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.3390/jcm12155107" } }, { "@type": "ScholarlyArticle", "name": "Contribution of Nutritional, Lifestyle, and Metabolic Risk Factors to Parkinson's Disease.", "datePublished": "2024-03-26", "url": "https://recherchemedicale.com/article/38532309", "identifier": { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.1002/mds.29778" } }, { "@type": "ScholarlyArticle", "name": "Nutritional metabolism and cerebral bioenergetics in Alzheimer's disease and related dementias.", "datePublished": "2022-12-08", "url": "https://recherchemedicale.com/article/36479795", "identifier": { "@type": "PropertyValue", "propertyID": "DOI", "value": "10.1002/alz.12845" } } ], "breadcrumb": { "@type": "BreadcrumbList", "itemListElement": [ { "@type": "ListItem", "position": 1, "name": "Recherchemedicale.com", "item": "https://recherchemedicale.com" }, { "@type": "ListItem", "position": 2, "name": "Maladies métaboliques et nutritionnelles", "item": "https://recherchemedicale.com/mesh/D009750" } ] } }, { "@type": "MedicalWebPage", "name": "Article complet : Maladies métaboliques et nutritionnelles - Questions et réponses", "headline": "Questions et réponses médicales fréquentes sur Maladies métaboliques et nutritionnelles", "description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.", "datePublished": "2025-01-22", "inLanguage": "fr", "hasPart": [ { "@type": "MedicalWebPage", "name": "Diagnostic", "headline": "Diagnostic sur Maladies métaboliques et nutritionnelles", "description": "Comment diagnostiquer le diabète de type 2 ?\nQuels tests pour l'hyperlipidémie ?\nComment détecter une carence en fer ?\nQuels signes indiquent une maladie de Wilson ?\nComment évaluer l'obésité ?", "url": "https://recherchemedicale.com/mesh/D009750#section-diagnostic" }, { "@type": "MedicalWebPage", "name": "Symptômes", "headline": "Symptômes sur Maladies métaboliques et nutritionnelles", "description": "Quels sont les symptômes du diabète ?\nComment se manifeste l'hyperthyroïdie ?\nQuels signes d'une carence en vitamine D ?\nQuels symptômes de l'acidocétose diabétique ?\nComment reconnaître une hypoglycémie ?", "url": "https://recherchemedicale.com/mesh/D009750#section-symptômes" }, { "@type": "MedicalWebPage", "name": "Prévention", "headline": "Prévention sur Maladies métaboliques et nutritionnelles", "description": "Comment prévenir le diabète de type 2 ?\nQuelles mesures pour éviter l'obésité ?\nComment prévenir les carences nutritionnelles ?\nQuelles stratégies pour éviter l'hyperlipidémie ?\nComment prévenir l'acidocétose diabétique ?", "url": "https://recherchemedicale.com/mesh/D009750#section-prévention" }, { "@type": "MedicalWebPage", "name": "Traitements", "headline": "Traitements sur Maladies métaboliques et nutritionnelles", "description": "Quel traitement pour le diabète de type 1 ?\nComment traiter l'hyperlipidémie ?\nQuel est le traitement de l'obésité ?\nComment traiter une carence en fer ?\nQuel traitement pour l'hyperthyroïdie ?", "url": "https://recherchemedicale.com/mesh/D009750#section-traitements" }, { "@type": "MedicalWebPage", "name": "Complications", "headline": "Complications sur Maladies métaboliques et nutritionnelles", "description": "Quelles complications du diabète ?\nQuels risques liés à l'obésité ?\nQuelles complications de l'hyperlipidémie ?\nQuels effets d'une carence en vitamine D ?\nQuelles complications de l'hyperthyroïdie ?", "url": "https://recherchemedicale.com/mesh/D009750#section-complications" }, { "@type": "MedicalWebPage", "name": "Facteurs de risque", "headline": "Facteurs de risque sur Maladies métaboliques et nutritionnelles", "description": "Quels facteurs de risque pour le diabète ?\nQuels risques liés à l'alimentation pour l'hyperlipidémie ?\nQuels facteurs de risque pour l'obésité ?\nQuels risques de carence en fer ?\nQuels facteurs de risque pour l'hyperthyroïdie ?", "url": "https://recherchemedicale.com/mesh/D009750#section-facteurs de risque" } ] }, { "@type": "FAQPage", "mainEntity": [ { "@type": "Question", "name": "Comment diagnostiquer le diabète de type 2 ?", "position": 1, "acceptedAnswer": { "@type": "Answer", "text": "Le diagnostic se fait par des tests de glycémie à jeun et l'HbA1c." } }, { "@type": "Question", "name": "Quels tests pour l'hyperlipidémie ?", "position": 2, "acceptedAnswer": { "@type": "Answer", "text": "Un profil lipidique sanguin mesure les niveaux de cholestérol et triglycérides." } }, { "@type": "Question", "name": "Comment détecter une carence en fer ?", "position": 3, "acceptedAnswer": { "@type": "Answer", "text": "Des tests sanguins mesurent la ferritine et l'hémoglobine." } }, { "@type": "Question", "name": "Quels signes indiquent une maladie de Wilson ?", "position": 4, "acceptedAnswer": { "@type": "Answer", "text": "Des tests de cuivre sérique et une biopsie hépatique confirment la maladie." } }, { "@type": "Question", "name": "Comment évaluer l'obésité ?", "position": 5, "acceptedAnswer": { "@type": "Answer", "text": "L'IMC (indice de masse corporelle) est utilisé pour évaluer l'obésité." } }, { "@type": "Question", "name": "Quels sont les symptômes du diabète ?", "position": 6, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes incluent soif excessive, urination fréquente et fatigue." } }, { "@type": "Question", "name": "Comment se manifeste l'hyperthyroïdie ?", "position": 7, "acceptedAnswer": { "@type": "Answer", "text": "Elle se manifeste par perte de poids, nervosité et palpitations." } }, { "@type": "Question", "name": "Quels signes d'une carence en vitamine D ?", "position": 8, "acceptedAnswer": { "@type": "Answer", "text": "Les signes incluent fatigue, douleurs osseuses et faiblesse musculaire." } }, { "@type": "Question", "name": "Quels symptômes de l'acidocétose diabétique ?", "position": 9, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes incluent nausées, vomissements et respiration rapide." } }, { "@type": "Question", "name": "Comment reconnaître une hypoglycémie ?", "position": 10, "acceptedAnswer": { "@type": "Answer", "text": "Les signes incluent tremblements, sueurs et confusion mentale." } }, { "@type": "Question", "name": "Comment prévenir le diabète de type 2 ?", "position": 11, "acceptedAnswer": { "@type": "Answer", "text": "Un mode de vie sain avec une alimentation équilibrée et de l'exercice aide." } }, { "@type": "Question", "name": "Quelles mesures pour éviter l'obésité ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "Maintenir un poids santé par l'alimentation et l'activité physique régulière." } }, { "@type": "Question", "name": "Comment prévenir les carences nutritionnelles ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Une alimentation variée et équilibrée est essentielle pour éviter les carences." } }, { "@type": "Question", "name": "Quelles stratégies pour éviter l'hyperlipidémie ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Adopter un régime pauvre en graisses saturées et faire de l'exercice régulièrement." } }, { "@type": "Question", "name": "Comment prévenir l'acidocétose diabétique ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Un bon contrôle de la glycémie et une éducation sur le diabète sont cruciaux." } }, { "@type": "Question", "name": "Quel traitement pour le diabète de type 1 ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Le traitement principal est l'insulinothérapie pour réguler la glycémie." } }, { "@type": "Question", "name": "Comment traiter l'hyperlipidémie ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "Les statines et un régime alimentaire adapté sont souvent prescrits." } }, { "@type": "Question", "name": "Quel est le traitement de l'obésité ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "Le traitement inclut un régime, de l'exercice et parfois des médicaments." } }, { "@type": "Question", "name": "Comment traiter une carence en fer ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Des suppléments de fer et des modifications alimentaires sont recommandés." } }, { "@type": "Question", "name": "Quel traitement pour l'hyperthyroïdie ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements incluent des médicaments antithyroïdiens ou l'iode radioactif." } }, { "@type": "Question", "name": "Quelles complications du diabète ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Les complications incluent neuropathie, rétinopathie et maladies cardiovasculaires." } }, { "@type": "Question", "name": "Quels risques liés à l'obésité ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "L'obésité augmente le risque de maladies cardiaques, diabète et hypertension." } }, { "@type": "Question", "name": "Quelles complications de l'hyperlipidémie ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Elle peut entraîner des maladies coronariennes et des AVC." } }, { "@type": "Question", "name": "Quels effets d'une carence en vitamine D ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Une carence peut causer des troubles osseux et un affaiblissement du système immunitaire." } }, { "@type": "Question", "name": "Quelles complications de l'hyperthyroïdie ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Les complications incluent l'ostéoporose et les troubles cardiaques." } }, { "@type": "Question", "name": "Quels facteurs de risque pour le diabète ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "L'obésité, l'inactivité physique et des antécédents familiaux augmentent le risque." } }, { "@type": "Question", "name": "Quels risques liés à l'alimentation pour l'hyperlipidémie ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Une alimentation riche en graisses saturées et en sucres augmente le risque." } }, { "@type": "Question", "name": "Quels facteurs de risque pour l'obésité ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Les facteurs incluent la génétique, le mode de vie et des troubles hormonaux." } }, { "@type": "Question", "name": "Quels risques de carence en fer ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Les régimes végétariens stricts et les pertes sanguines augmentent le risque." } }, { "@type": "Question", "name": "Quels facteurs de risque pour l'hyperthyroïdie ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Les antécédents familiaux et certaines maladies auto-immunes augmentent le risque." } } ] } ] }
Dr Olivier Menir

Contenu validé par Dr Olivier Menir

Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale

Validation scientifique effectuée le 03/11/2024

Contenu vérifié selon les dernières recommandations médicales

En savoir plus sur Dr Menir

Sous-catégories

305 au total
└─

Maladies métaboliques

Metabolic Diseases D008659 - C18.452
└─

Troubles nutritionnels

Nutrition Disorders D009748 - C18.654
└─└─

Troubles de l'équilibre acidobasique

Acid-Base Imbalance D000137 - C18.452.076
└─└─

Maladies osseuses métaboliques

Bone Diseases, Metabolic D001851 - C18.452.104
└─└─

Encéphalopathies métaboliques

Brain Diseases, Metabolic D001928 - C18.452.132
└─└─

Troubles du métabolisme du calcium

Calcium Metabolism Disorders D002128 - C18.452.174
└─└─

Troubles dus à un défaut de réparation de l'ADN

DNA Repair-Deficiency Disorders D049914 - C18.452.284
└─└─

Troubles du métabolisme du glucose

Glucose Metabolism Disorders D044882 - C18.452.394
└─└─

Troubles du métabolisme du fer

Iron Metabolism Disorders D019189 - C18.452.565
└─└─

Troubles du métabolisme lipidique

Lipid Metabolism Disorders D052439 - C18.452.584
└─└─

Syndromes de malabsorption

Malabsorption Syndromes D008286 - C18.452.603
└─└─

Syndrome métabolique X

Metabolic Syndrome D024821 - C18.452.625
└─└─

Erreurs innées du métabolisme

Metabolism, Inborn Errors D008661 - C18.452.648
└─└─

Maladies mitochondriales

Mitochondrial Diseases D028361 - C18.452.660
└─└─

Troubles du métabolisme du phosphore

Phosphorus Metabolism Disorders D010760 - C18.452.750
└─└─

Porphyries

Porphyrias D011164 - C18.452.811
└─└─

Troubles de l'homéostasie des protéines

Proteostasis Deficiencies D057165 - C18.452.845
└─└─

Dermatoses métaboliques

Skin Diseases, Metabolic D012875 - C18.452.880
└─└─

Troubles de l'équilibre hydroélectrolytique

Water-Electrolyte Imbalance D014883 - C18.452.950
└─└─

Troubles nutritionnels de l'enfant

Child Nutrition Disorders D015362 - C18.654.180
└─└─

Hypervitaminose A

Hypervitaminosis A D006986 - C18.654.301
└─└─

Troubles nutritionnels du nourrisson

Infant Nutrition Disorders D007228 - C18.654.422
└─└─

Malnutrition

Malnutrition D044342 - C18.654.521
└─└─

Surnutrition

Overnutrition D044343 - C18.654.726
└─└─

Syndrome cachectique

Wasting Syndrome D019282 - C18.654.940
└─└─└─

Achlorhydrie

Achlorhydria D000126 - C18.452.076.087
└─└─└─

Acidose

Acidosis D000138 - C18.452.076.176
└─└─└─

Alcalose

Alkalosis D000471 - C18.452.076.354
└─└─└─

Déminéralisation osseuse pathologique

Bone Demineralization, Pathologic D018488 - C18.452.104.247
└─└─└─

Ostéoporose

Osteoporosis D010024 - C18.452.104.579
└─└─└─

Encéphalopathie hépatique

Hepatic Encephalopathy D006501 - C18.452.132.360
└─└─└─

Myélinolyse centropontine

Myelinolysis, Central Pontine D017590 - C18.452.132.560
└─└─└─

Syndrome de Reye

Reye Syndrome D012202 - C18.452.132.780
└─└─└─

Calcinose

Calcinosis D002114 - C18.452.174.130
└─└─└─

Décalcification osseuse

Decalcification, Pathologic D003649 - C18.452.174.289
└─└─└─

Syndrome de Cockayne

Cockayne Syndrome D003057 - C18.452.284.250
└─└─└─

Tumeurs colorectales héréditaires sans polypose

Colorectal Neoplasms, Hereditary Nonpolyposis D003123 - C18.452.284.255
└─└─└─

Anémie de Fanconi

Fanconi Anemia D005199 - C18.452.284.280
└─└─└─

Syndrome de Li-Fraumeni

Li-Fraumeni Syndrome D016864 - C18.452.284.520
└─└─└─

Syndrome des cassures de Nijmegen

Nijmegen Breakage Syndrome D049932 - C18.452.284.600
└─└─└─

Syndrome de Rothmund-Thomson

Rothmund-Thomson Syndrome D011038 - C18.452.284.760
└─└─└─

Syndrome de Werner

Werner Syndrome D014898 - C18.452.284.960
└─└─└─

Xeroderma pigmentosum

Xeroderma Pigmentosum D014983 - C18.452.284.975
└─└─└─

Glycosurie

Glycosuria D006029 - C18.452.394.937
└─└─└─

Hyperglycémie

Hyperglycemia D006943 - C18.452.394.952
└─└─└─

Hyperinsulinisme

Hyperinsulinism D006946 - C18.452.394.968
└─└─└─

Hypoglycémie

Hypoglycemia D007003 - C18.452.394.984
└─└─└─

Hyperferritinémie

Hyperferritinemia D000085583 - C18.452.565.300
└─└─└─

Carences en fer

Iron Deficiencies D000090463 - C18.452.565.400
└─└─└─

Surcharge en fer

Iron Overload D019190 - C18.452.565.500
└─└─└─

Dyslipidémies

Dyslipidemias D050171 - C18.452.584.500
└─└─└─

Lipomatose

Lipomatosis D008068 - C18.452.584.718
└─└─└─

Xanthomatose

Xanthomatosis D014973 - C18.452.584.750
└─└─└─

Syndrome de l'anse borgne

Blind Loop Syndrome D001765 - C18.452.603.145
└─└─└─

Maladie coeliaque

Celiac Disease D002446 - C18.452.603.250
└─└─└─

Sprue collagène

Collagenous Sprue D064068 - C18.452.603.314
└─└─└─

Sprue tropicale

Sprue, Tropical D013182 - C18.452.603.850
└─└─└─

Stéatorrhée

Steatorrhea D045602 - C18.452.603.887
└─└─└─

Maladie de Whipple

Whipple Disease D008061 - C18.452.603.925
└─└─└─

Aminoacidopathies congénitales

Amino Acid Metabolism, Inborn Errors D000592 - C18.452.648.100
└─└─└─

Troubles congénitaux du transport des acides aminés

Amino Acid Transport Disorders, Inborn D020157 - C18.452.648.151
└─└─└─

Encéphalopathies métaboliques congénitales

Brain Diseases, Metabolic, Inborn D020739 - C18.452.648.189
└─└─└─

Erreurs innées du métabolisme glucidique

Carbohydrate Metabolism, Inborn Errors D002239 - C18.452.648.202
└─└─└─

Hyperbilirubinémie héréditaire

Hyperbilirubinemia, Hereditary D006933 - C18.452.648.300
└─└─└─

Erreurs innées du métabolisme lipidique

Lipid Metabolism, Inborn Errors D008052 - C18.452.648.398
└─└─└─

Maladies lysosomiales

Lysosomal Storage Diseases D016464 - C18.452.648.595
└─└─└─

Erreurs innées du métabolisme des métaux

Metal Metabolism, Inborn Errors D008664 - C18.452.648.618
└─└─└─

Maladies péroxysomiales

Peroxisomal Disorders D018901 - C18.452.648.663
└─└─└─

Progeria

Progeria D011371 - C18.452.648.753
└─└─└─

Erreurs innées du métabolisme de la purine et de la pyrimidine

Purine-Pyrimidine Metabolism, Inborn Errors D011686 - C18.452.648.798
└─└─└─

Erreurs innées du transport tubulaire rénal

Renal Tubular Transport, Inborn Errors D015499 - C18.452.648.893
└─└─└─

Erreurs innées du métabolisme des stéroïdes

Steroid Metabolism, Inborn Errors D043202 - C18.452.648.925
└─└─└─

Déficit en carbamoyl-phosphate synthase I

Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 - C18.452.660.097
└─└─└─

Déficit en cytochrome-c oxydase

Cytochrome-c Oxidase Deficiency D030401 - C18.452.660.195
└─└─└─

Ataxie de Friedreich

Friedreich Ataxia D005621 - C18.452.660.300
└─└─└─

Maladie de Leigh

Leigh Disease D007888 - C18.452.660.520
└─└─└─

Myopathies mitochondriales

Mitochondrial Myopathies D017240 - C18.452.660.560
└─└─└─

Déficit multiple en acyl CoA déshydrogénase

Multiple Acyl Coenzyme A Dehydrogenase Deficiency D054069 - C18.452.660.612
└─└─└─

Atrophie optique autosomique dominante

Optic Atrophy, Autosomal Dominant D029241 - C18.452.660.665
└─└─└─

Atrophie optique héréditaire de Leber

Optic Atrophy, Hereditary, Leber D029242 - C18.452.660.670
└─└─└─

Déficit en pyruvate carboxylase

Pyruvate Carboxylase Deficiency Disease D015324 - C18.452.660.705
└─└─└─

Déficit en complexe pyruvate-déshydrogénase

Pyruvate Dehydrogenase Complex Deficiency Disease D015325 - C18.452.660.710
└─└─└─

Hyperphosphatémie

Hyperphosphatemia D054559 - C18.452.750.199
└─└─└─

Hypophosphatémie

Hypophosphatemia D017674 - C18.452.750.400
└─└─└─

Porphyrie érythropoïétique

Porphyria, Erythropoietic D017092 - C18.452.811.250
└─└─└─

Porphyries hépatiques

Porphyrias, Hepatic D017094 - C18.452.811.400
└─└─└─

Amyloïdose

Amyloidosis D000686 - C18.452.845.500
└─└─└─

Synucléinopathies

Synucleinopathies D000080874 - C18.452.845.650
└─└─└─

Protéinopathies TDP-43

TDP-43 Proteinopathies D057177 - C18.452.845.800
└─└─└─

Lipodystrophie

Lipodystrophy D008060 - C18.452.880.391
└─└─└─

Nécrobiose lipoïdique

Necrobiosis Lipoidica D009335 - C18.452.880.495
└─└─└─

Hypercalcémie

Hypercalcemia D006934 - C18.452.950.340
└─└─└─

Hyperkaliémie

Hyperkalemia D006947 - C18.452.950.396
└─└─└─

Hypernatrémie

Hypernatremia D006955 - C18.452.950.452
└─└─└─

Hypocalcémie

Hypocalcemia D006996 - C18.452.950.509
└─└─└─

Hypokaliémie

Hypokalemia D007008 - C18.452.950.565
└─└─└─

Hyponatrémie

Hyponatremia D007010 - C18.452.950.620
└─└─└─

Maladies de carence

Deficiency Diseases D003677 - C18.654.521.500
└─└─└─

Troubles nutritionnels du foetus

Fetal Nutrition Disorders D048070 - C18.654.521.625
└─└─└─

Syndrome de renutrition

Refeeding Syndrome D055677 - C18.654.521.687
└─└─└─

Malnutrition aigüe sévère

Severe Acute Malnutrition D000067011 - C18.654.521.719
└─└─└─

Inanition

Starvation D013217 - C18.654.521.750
└─└─└─└─

Acidose lactique

Acidosis, Lactic D000140 - C18.452.076.176.180
└─└─└─└─

Acidose tubulaire rénale

Acidosis, Renal Tubular D000141 - C18.452.076.176.210
└─└─└─└─

Acidose respiratoire

Acidosis, Respiratory D000142 - C18.452.076.176.310
└─└─└─└─

Cétose

Ketosis D007662 - C18.452.076.176.652
└─└─└─└─

Alcalose respiratoire

Alkalosis, Respiratory D000472 - C18.452.076.354.271
└─└─└─└─

Ostéoporose post-ménopausique

Osteoporosis, Postmenopausal D015663 - C18.452.104.579.610
└─└─└─└─

Calcinose cutanée

Calcinosis Cutis D000092182 - C18.452.174.130.093
└─└─└─└─

Calciphylaxie

Calciphylaxis D002115 - C18.452.174.130.186
└─└─└─└─

Syndrome CREST

CREST Syndrome D017675 - C18.452.174.130.204
└─└─└─└─

Néphrocalcinose

Nephrocalcinosis D009397 - C18.452.174.130.560
└─└─└─└─

Calcification vasculaire

Vascular Calcification D061205 - C18.452.174.130.780
└─└─└─└─

Glycosurie rénale

Glycosuria, Renal D006030 - C18.452.394.937.450
└─└─└─└─

Intolérance au glucose

Glucose Intolerance D018149 - C18.452.394.952.500
└─└─└─└─

Hyperinsulinisme congénital

Congenital Hyperinsulinism D044903 - C18.452.394.984.200
└─└─└─└─

Coma insulinique

Insulin Coma D007331 - C18.452.394.984.492
└─└─└─└─

Anémie par carence en fer

Anemia, Iron-Deficiency D018798 - C18.452.565.400.500
└─└─└─└─

Hémosidérose

Hemosiderosis D006486 - C18.452.565.500.500
└─└─└─└─

Hyperlipidémies

Hyperlipidemias D006949 - C18.452.584.500.500
└─└─└─└─

Hypobêtalipoprotéinémie familiale

Hypobetalipoproteinemia, Familial, Apolipoprotein B D052476 - C18.452.584.563.497
└─└─└─└─

Adipose douloureuse

Adiposis Dolorosa D000274 - C18.452.584.718.500
└─└─└─└─

Lipomatose familiale

Familial Multiple Lipomatosis D000071070 - C18.452.584.718.625
└─└─└─└─

Adénolipomatose symétrique à prédominance cervicale

Lipomatosis, Multiple Symmetrical D008069 - C18.452.584.718.750
└─└─└─└─

Maladie de Shwachman

Shwachman-Diamond Syndrome D000081003 - C18.452.584.718.875
└─└─└─└─

Albinisme

Albinism D000417 - C18.452.648.100.102
└─└─└─└─

Alcaptonurie

Alkaptonuria D000474 - C18.452.648.100.187
└─└─└─└─

Acidémie propionique

Propionic Acidemia D056693 - C18.452.648.100.823
└─└─└─└─

Maladie de Hartnup

Hartnup Disease D006250 - C18.452.648.189.355
└─└─└─└─

Maladies démyélinisantes héréditaires du système nerveux central

Hereditary Central Nervous System Demyelinating Diseases D020279 - C18.452.648.189.362
└─└─└─└─

Homocystinurie

Homocystinuria D006712 - C18.452.648.189.365
└─└─└─└─

Hyperglycinémie non cétosique

Hyperglycinemia, Nonketotic D020158 - C18.452.648.189.375
└─└─└─└─

Hyperlysinémies

Hyperlysinemias D020167 - C18.452.648.189.380
└─└─└─└─

Leucinose

Maple Syrup Urine Disease D008375 - C18.452.648.189.520
└─└─└─└─

Syndrome de Lowe

Oculocerebrorenal Syndrome D009800 - C18.452.648.189.640
└─└─└─└─

Phénylcétonuries

Phenylketonurias D010661 - C18.452.648.189.687
└─└─└─└─

Tyrosinémies

Tyrosinemias D020176 - C18.452.648.189.875
└─└─└─└─

Anomalies congénitales du cycle de l'urée

Urea Cycle Disorders, Inborn D056806 - C18.452.648.189.937
└─└─└─└─

Troubles congénitaux de la glycosylation

Congenital Disorders of Glycosylation D018981 - C18.452.648.202.125
└─└─└─└─

Erreurs innées du métabolisme du fructose

Fructose Metabolism, Inborn Errors D015318 - C18.452.648.202.251
└─└─└─└─

Galactosémies

Galactosemias D005693 - C18.452.648.202.355
└─└─└─└─

Déficit en glucose-6-phosphate-déshydrogénase

Glucosephosphate Dehydrogenase Deficiency D005955 - C18.452.648.202.402
└─└─└─└─

Glycogénose

Glycogen Storage Disease D006008 - C18.452.648.202.449
└─└─└─└─

Hyperoxalurie primaire

Hyperoxaluria, Primary D006960 - C18.452.648.202.460
└─└─└─└─

Intolérance au lactose

Lactose Intolerance D007787 - C18.452.648.202.589
└─└─└─└─

Déficit multiple en carboxylases

Multiple Carboxylase Deficiency D009100 - C18.452.648.202.720
└─└─└─└─

Erreurs innées du métabolisme du pyruvate

Pyruvate Metabolism, Inborn Errors D015323 - C18.452.648.202.810
└─└─└─└─

Syndrome de Crigler-Najjar

Crigler-Najjar Syndrome D003414 - C18.452.648.300.281
└─└─└─└─

Maladie de Gilbert

Gilbert Disease D005878 - C18.452.648.300.528
└─└─└─└─

Syndrome de Barth

Barth Syndrome D056889 - C18.452.648.398.224
└─└─└─└─

Hyperlipidémie familiale mixte

Hyperlipidemia, Familial Combined D006950 - C18.452.648.398.450
└─└─└─└─

Hyperlipoprotéinémie de type I

Hyperlipoproteinemia Type I D008072 - C18.452.648.398.465
└─└─└─└─

Hyperlipoprotéinémie de type II

Hyperlipoproteinemia Type II D006938 - C18.452.648.398.481
└─└─└─└─

Hyperlipoprotéinémie de type III

Hyperlipoproteinemia Type III D006952 - C18.452.648.398.483
└─└─└─└─

Hyperlipoprotéinémie de type IV

Hyperlipoproteinemia Type IV D006953 - C18.452.648.398.487
└─└─└─└─

Hyperlipoprotéinémie de type V

Hyperlipoproteinemia Type V D006954 - C18.452.648.398.493
└─└─└─└─

Hypolipoprotéinémies

Hypolipoproteinemias D007009 - C18.452.648.398.500
└─└─└─└─

Lipidoses

Lipidoses D008064 - C18.452.648.398.641
└─└─└─└─

Xanthomatose cérébrotendineuse

Xanthomatosis, Cerebrotendinous D019294 - C18.452.648.398.925
└─└─└─└─

Aspartylglucosaminurie

Aspartylglucosaminuria D054880 - C18.452.648.595.100
└─└─└─└─

Maladie de stockage des esters de cholestérol

Cholesterol Ester Storage Disease D015217 - C18.452.648.595.201
└─└─└─└─

Cystinose

Cystinosis D003554 - C18.452.648.595.377
└─└─└─└─

Maladies neurologiques de surcharge lysosomiale

Lysosomal Storage Diseases, Nervous System D020140 - C18.452.648.595.554
└─└─└─└─

Mannosidoses

Mannosidase Deficiency Diseases D044904 - C18.452.648.595.577
└─└─└─└─

Mucopolysaccharidoses

Mucopolysaccharidoses D009083 - C18.452.648.595.600
└─└─└─└─

Pycnodysostose

Pycnodysostosis D058631 - C18.452.648.595.800
└─└─└─└─

Hémochromatose

Hemochromatosis D006432 - C18.452.648.618.337
└─└─└─└─

Dégénérescence hépatolenticulaire

Hepatolenticular Degeneration D006527 - C18.452.648.618.403
└─└─└─└─

Hypophosphatasie

Hypophosphatasia D007014 - C18.452.648.618.482
└─└─└─└─

Maladie de Menkès

Menkes Kinky Hair Syndrome D007706 - C18.452.648.618.590
└─└─└─└─

Paralysies périodiques familiales

Paralyses, Familial Periodic D010245 - C18.452.648.618.711
└─└─└─└─

Pseudohypoparathyroïdie

Pseudohypoparathyroidism D011547 - C18.452.648.618.815
└─└─└─└─

Acatalasie

Acatalasia D020642 - C18.452.648.663.050
└─└─└─└─

Chondrodysplasie ponctuée rhizomélique

Chondrodysplasia Punctata, Rhizomelic D018902 - C18.452.648.663.265
└─└─└─└─

Maladie de Refsum

Refsum Disease D012035 - C18.452.648.663.760
└─└─└─└─

Maladie de Refsum infantile

Refsum Disease, Infantile D052919 - C18.452.648.663.865
└─└─└─└─

Syndrome de Zellweger

Zellweger Syndrome D015211 - C18.452.648.663.970
└─└─└─└─

Déficit en dihydropyrimidine déshydrogénase

Dihydropyrimidine Dehydrogenase Deficiency D054067 - C18.452.648.798.183
└─└─└─└─

Goutte

Gout D006073 - C18.452.648.798.368
└─└─└─└─

Syndrome de Lesch-Nyhan

Lesch-Nyhan Syndrome D007926 - C18.452.648.798.594
└─└─└─└─

Phénotype du syndrome d'Antley-Bixler

Antley-Bixler Syndrome Phenotype D054882 - C18.452.648.925.324
└─└─└─└─

Ichtyose liée à l'X

Ichthyosis, X-Linked D016114 - C18.452.648.925.400
└─└─└─└─

Syndrome d'excès apparent en minéralocorticoïdes

Mineralocorticoid Excess Syndrome, Apparent D043204 - C18.452.648.925.500
└─└─└─└─

Syndrome de Smith-Lemli-Optiz

Smith-Lemli-Opitz Syndrome D019082 - C18.452.648.925.875
└─└─└─└─

Encéphalomyopathies mitochondriales

Mitochondrial Encephalomyopathies D017237 - C18.452.660.560.620
└─└─└─└─

Hypophosphatémie familiale

Hypophosphatemia, Familial D007015 - C18.452.750.400.500
└─└─└─└─

Coproporphyrie héréditaire

Coproporphyria, Hereditary D046349 - C18.452.811.400.074
└─└─└─└─

Porphyrie aigüe intermittente

Porphyria, Acute Intermittent D017118 - C18.452.811.400.150
└─└─└─└─

Porphyrie cutanée tardive

Porphyria Cutanea Tarda D017119 - C18.452.811.400.250
└─└─└─└─

Porphyrie hépatoérythropoïétique

Porphyria, Hepatoerythropoietic D017121 - C18.452.811.400.437
└─└─└─└─

Porphyrie variegata

Porphyria, Variegate D046350 - C18.452.811.400.625
└─└─└─└─

Protoporphyrie érythropoïétique

Protoporphyria, Erythropoietic D046351 - C18.452.811.400.812
└─└─└─└─

Neuropathies amyloïdes

Amyloid Neuropathies D017772 - C18.452.845.500.050
└─└─└─└─

Amyloïdose familiale

Amyloidosis, Familial D028226 - C18.452.845.500.075
└─└─└─└─

Angiopathie amyloïde cérébrale

Cerebral Amyloid Angiopathy D016657 - C18.452.845.500.100
└─└─└─└─

Sclérose latérale amyotrophique

Amyotrophic Lateral Sclerosis D000690 - C18.452.845.800.050
└─└─└─└─

Lipodystrophie généralisée congénitale

Lipodystrophy, Congenital Generalized D052497 - C18.452.880.391.550
└─└─└─└─

Lipodystrophie partielle familiale

Lipodystrophy, Familial Partial D052496 - C18.452.880.391.700
└─└─└─└─

Avitaminoses

Avitaminosis D001361 - C18.654.521.500.133
└─└─└─└─

Magnésium, carence

Magnesium Deficiency D008275 - C18.654.521.500.439
└─└─└─└─

Potassium, carence

Potassium Deficiency D011191 - C18.654.521.500.617
└─└─└─└─

Carence protéique

Protein Deficiency D011488 - C18.654.521.500.708
└─└─└─└─

Kwashiorkor

Kwashiorkor D007732 - C18.654.521.719.500
└─└─└─└─└─

Sclérose de Mönckeberg

Monckeberg Medial Calcific Sclerosis D050380 - C18.452.174.130.780.500
└─└─└─└─└─

Nésidioblastose

Nesidioblastosis D046768 - C18.452.394.984.200.500
└─└─└─└─└─

Hypercholestérolémie

Hypercholesterolemia D006937 - C18.452.584.500.500.396
└─└─└─└─└─

Hyperlipoprotéinémies

Hyperlipoproteinemias D006951 - C18.452.584.500.500.644
└─└─└─└─└─

Hypertriglycéridémie

Hypertriglyceridemia D015228 - C18.452.584.500.500.851
└─└─└─└─└─

Albinisme oculaire

Albinism, Ocular D016117 - C18.452.648.100.102.090
└─└─└─└─└─

Albinisme oculocutané

Albinism, Oculocutaneous D016115 - C18.452.648.100.102.100
└─└─└─└─└─

Piébaldisme

Piebaldism D016116 - C18.452.648.100.102.600
└─└─└─└─└─

Maladie d'Alexander

Alexander Disease D038261 - C18.452.648.189.362.312
└─└─└─└─└─

Maladie de Canavan

Canavan Disease D017825 - C18.452.648.189.362.375
└─└─└─└─└─

Maladie de Pelizaeus-Merzbacher

Pelizaeus-Merzbacher Disease D020371 - C18.452.648.189.362.775
└─└─└─└─└─

Phénylcétonurie maternelle

Phenylketonuria, Maternal D017042 - C18.452.648.189.687.500
└─└─└─└─└─

Acidurie arginosuccinique

Argininosuccinic Aciduria D056807 - C18.452.648.189.937.124
└─└─└─└─└─

Citrullinémie

Citrullinemia D020159 - C18.452.648.189.937.374
└─└─└─└─└─

Hyperargininémie

Hyperargininemia D020162 - C18.452.648.189.937.437
└─└─└─└─└─

Déficit en ornithine carbamyl transférase

Ornithine Carbamoyltransferase Deficiency Disease D020163 - C18.452.648.189.937.500
└─└─└─└─└─

Déficit en fructose-1,6-diphosphatase

Fructose-1,6-Diphosphatase Deficiency D015319 - C18.452.648.202.251.221
└─└─└─└─└─

Intolérance au fructose

Fructose Intolerance D005633 - C18.452.648.202.251.271
└─└─└─└─└─

Glycogénose de type I

Glycogen Storage Disease Type I D005953 - C18.452.648.202.449.448
└─└─└─└─└─

Glycogénose de type IIb

Glycogen Storage Disease Type IIb D052120 - C18.452.648.202.449.510
└─└─└─└─└─

Glycogénose de type III

Glycogen Storage Disease Type III D006010 - C18.452.648.202.449.520
└─└─└─└─└─

Glycogénose de type IV

Glycogen Storage Disease Type IV D006011 - C18.452.648.202.449.540
└─└─└─└─└─

Glycogénose de type V

Glycogen Storage Disease Type V D006012 - C18.452.648.202.449.560
└─└─└─└─└─

Glycogénose de type VI

Glycogen Storage Disease Type VI D006013 - C18.452.648.202.449.580
└─└─└─└─└─

Glycogénose de type VII

Glycogen Storage Disease Type VII D006014 - C18.452.648.202.449.600
└─└─└─└─└─

Glycogénose de type VIII

Glycogen Storage Disease Type VIII D006015 - C18.452.648.202.449.620
└─└─└─└─└─

Déficit en biotinidase

Biotinidase Deficiency D028921 - C18.452.648.202.720.100
└─└─└─└─└─

Déficit en holocarboxylase synthétase

Holocarboxylase Synthetase Deficiency D028922 - C18.452.648.202.720.380
└─└─└─└─└─

Hypercholestérolémie familiale homozygote

Homozygous Familial Hypercholesterolemia D000090542 - C18.452.648.398.481.500
└─└─└─└─└─

Hypoalphalipoprotéinémies

Hypoalphalipoproteinemias D052456 - C18.452.648.398.500.330
└─└─└─└─└─

Hypobêtalipoprotéinémies

Hypobetalipoproteinemias D006995 - C18.452.648.398.500.440
└─└─└─└─└─

Céroïdes-lipofuscinoses neuronales

Neuronal Ceroid-Lipofuscinoses D009472 - C18.452.648.398.641.509
└─└─└─└─└─

Syndrome de Sjögren-Larsson

Sjogren-Larsson Syndrome D016111 - C18.452.648.398.641.723
└─└─└─└─└─

Maladie de Wolman

Wolman Disease D015223 - C18.452.648.595.201.500
└─└─└─└─└─

Fucosidose

Fucosidosis D005645 - C18.452.648.595.554.295
└─└─└─└─└─

Glycogénose de type II

Glycogen Storage Disease Type II D006009 - C18.452.648.595.554.340
└─└─└─└─└─

Mucolipidoses

Mucolipidoses D009081 - C18.452.648.595.554.590
└─└─└─└─└─

Maladie de surcharge en acide sialique

Sialic Acid Storage Disease D029461 - C18.452.648.595.554.810
└─└─└─└─└─

Sphingolipidoses

Sphingolipidoses D013106 - C18.452.648.595.554.825
└─└─└─└─└─

alpha-Mannosidose

alpha-Mannosidosis D008363 - C18.452.648.595.577.500
└─└─└─└─└─

bêta-Mannosidose

beta-Mannosidosis D044905 - C18.452.648.595.577.750
└─└─└─└─└─

Mucopolysaccharidose de type I

Mucopolysaccharidosis I D008059 - C18.452.648.595.600.640
└─└─└─└─└─

Mucopolysaccharidose de type II

Mucopolysaccharidosis II D016532 - C18.452.648.595.600.645
└─└─└─└─└─

Mucopolysaccharidose de type III

Mucopolysaccharidosis III D009084 - C18.452.648.595.600.650
└─└─└─└─└─

Mucopolysaccharidose de type IV

Mucopolysaccharidosis IV D009085 - C18.452.648.595.600.655
└─└─└─└─└─

Mucopolysaccharidose de type VI

Mucopolysaccharidosis VI D009087 - C18.452.648.595.600.670
└─└─└─└─└─

Mucopolysaccharidose de type VII

Mucopolysaccharidosis VII D016538 - C18.452.648.595.600.675
└─└─└─└─└─

Paralysie périodique hypokaliémique

Hypokalemic Periodic Paralysis D020514 - C18.452.648.618.711.550
└─└─└─└─└─

Paralysie périodique hyperkaliémique

Paralysis, Hyperkalemic Periodic D020513 - C18.452.648.618.711.600
└─└─└─└─└─

Pseudopseudo-hypoparathyroïdie

Pseudopseudohypoparathyroidism D011556 - C18.452.648.618.815.815
└─└─└─└─└─

Goutte articulaire

Arthritis, Gouty D015210 - C18.452.648.798.368.410
└─└─└─└─└─

Syndrome MELAS

MELAS Syndrome D017241 - C18.452.660.560.620.520
└─└─└─└─└─

Syndrome MERRF

MERRF Syndrome D017243 - C18.452.660.560.620.530
└─└─└─└─└─

Neuropathies amyloïdes familiales

Amyloid Neuropathies, Familial D028227 - C18.452.845.500.075.050
└─└─└─└─└─

Angiopathie amyloïde cérébrale familiale

Cerebral Amyloid Angiopathy, Familial D028243 - C18.452.845.500.100.160
└─└─└─└─└─

Carence en acide ascorbique

Ascorbic Acid Deficiency D001206 - C18.654.521.500.133.115
└─└─└─└─└─

Carence en vitamine A

Vitamin A Deficiency D014802 - C18.654.521.500.133.628
└─└─└─└─└─

Carence en vitamines B

Vitamin B Deficiency D014804 - C18.654.521.500.133.699
└─└─└─└─└─

Carence en vitamine D

Vitamin D Deficiency D014808 - C18.654.521.500.133.770
└─└─└─└─└─

Carence en vitamine E

Vitamin E Deficiency D014811 - C18.654.521.500.133.841
└─└─└─└─└─

Carence en vitamine K

Vitamin K Deficiency D014813 - C18.654.521.500.133.912
└─└─└─└─└─

Malnutrition protéinocalorique

Protein-Energy Malnutrition D011502 - C18.654.521.500.708.626
└─└─└─└─└─

Syndrome obésité hypoventilation

Obesity Hypoventilation Syndrome D010845 - C18.654.726.750.500.600
└─└─└─└─└─

Syndrome de Prader-Willi

Prader-Willi Syndrome D011218 - C18.654.726.750.500.740
└─└─└─└─└─└─

Syndrome d'Hermanski-Pudlak

Hermanski-Pudlak Syndrome D022861 - C18.452.648.100.102.100.400
└─└─└─└─└─└─

Déficit en lécithine-cholestérol-acyl-transférase

Lecithin Cholesterol Acyltransferase Deficiency D007863 - C18.452.648.398.500.330.500
└─└─└─└─└─└─

Maladie de Tangier

Tangier Disease D013631 - C18.452.648.398.500.330.750
└─└─└─└─└─└─

Abêtalipoprotéinémie

Abetalipoproteinemia D000012 - C18.452.648.398.500.440.500
└─└─└─└─└─└─

Maladie de Fabry

Fabry Disease D000795 - C18.452.648.595.554.825.200
└─└─└─└─└─└─

Lipogranulomatose de Farber

Farber Lipogranulomatosis D055577 - C18.452.648.595.554.825.250
└─└─└─└─└─└─

Gangliosidoses

Gangliosidoses D005733 - C18.452.648.595.554.825.300
└─└─└─└─└─└─

Maladie de Gaucher

Gaucher Disease D005776 - C18.452.648.595.554.825.400
└─└─└─└─└─└─

Leucodystrophie à cellules globoïdes

Leukodystrophy, Globoid Cell D007965 - C18.452.648.595.554.825.590
└─└─└─└─└─└─

Maladies de Niemann-Pick

Niemann-Pick Diseases D009542 - C18.452.648.595.554.825.700
└─└─└─└─└─└─

Syndrome des histiocytes bleus de mer

Sea-Blue Histiocyte Syndrome D012618 - C18.452.648.595.554.825.775
└─└─└─└─└─└─

Sulfatidose

Sulfatidosis D052516 - C18.452.648.595.554.825.850
└─└─└─└─└─└─

Scorbut

Scurvy D012614 - C18.654.521.500.133.115.661
└─└─└─└─└─└─

Carence en choline

Choline Deficiency D002796 - C18.654.521.500.133.699.160
└─└─└─└─└─└─

Carence en acide folique

Folic Acid Deficiency D005494 - C18.654.521.500.133.699.308
└─└─└─└─└─└─

Hyperhomocystéinémie

Hyperhomocysteinemia D020138 - C18.654.521.500.133.699.418
└─└─└─└─└─└─

Pellagre

Pellagra D010383 - C18.654.521.500.133.699.529
└─└─└─└─└─└─

Carence en riboflavine

Riboflavin Deficiency D012257 - C18.654.521.500.133.699.713
└─└─└─└─└─└─

Carence en thiamine

Thiamine Deficiency D013832 - C18.654.521.500.133.699.827
└─└─└─└─└─└─

Carence en vitamine B6

Vitamin B 6 Deficiency D026681 - C18.654.521.500.133.699.901
└─└─└─└─└─└─

Carence en vitamine B12

Vitamin B 12 Deficiency D014806 - C18.654.521.500.133.699.923
└─└─└─└─└─└─

Rachitisme

Rickets D012279 - C18.654.521.500.133.770.734
└─└─└─└─└─└─

Saignement dû au déficit en vitamine K

Vitamin K Deficiency Bleeding D006475 - C18.654.521.500.133.912.360
└─└─└─└─└─└─└─

Gangliosidoses à GM2

Gangliosidoses, GM2 D020143 - C18.452.648.595.554.825.300.300
└─└─└─└─└─└─└─

Gangliosidose à GM1

Gangliosidosis, GM1 D016537 - C18.452.648.595.554.825.300.400
└─└─└─└─└─└─└─

Maladie de Niemann-Pick de type A

Niemann-Pick Disease, Type A D052536 - C18.452.648.595.554.825.700.500
└─└─└─└─└─└─└─

Maladie de Niemann-Pick de type B

Niemann-Pick Disease, Type B D052537 - C18.452.648.595.554.825.700.750
└─└─└─└─└─└─└─

Maladie de Niemann-Pick de type C

Niemann-Pick Disease, Type C D052556 - C18.452.648.595.554.825.700.875
└─└─└─└─└─└─└─

Leucodystrophie métachromatique

Leukodystrophy, Metachromatic D007966 - C18.452.648.595.554.825.850.500
└─└─└─└─└─└─└─

Déficit multiple en sulfatases

Multiple Sulfatase Deficiency Disease D052517 - C18.452.648.595.554.825.850.750
└─└─└─└─└─└─└─

Béribéri

Beriberi D001602 - C18.654.521.500.133.699.827.223
└─└─└─└─└─└─└─

Anémie pernicieuse

Anemia, Pernicious D000752 - C18.654.521.500.133.699.923.280
└─└─└─└─└─└─└─

Ostéomalacie

Osteomalacia D010018 - C18.654.521.500.133.770.734.640
└─└─└─└─└─└─└─

Rachitisme hypophosphatémique

Rickets, Hypophosphatemic D063730 - C18.654.521.500.133.770.734.875
└─└─└─└─└─└─└─└─

Maladie de Sandhoff

Sandhoff Disease D012497 - C18.452.648.595.554.825.300.300.800
└─└─└─└─└─└─└─└─

Maladie de Tay-Sachs

Tay-Sachs Disease D013661 - C18.452.648.595.554.825.300.300.840
└─└─└─└─└─└─└─└─

Maladie de Tay-Sachs variante AB

Tay-Sachs Disease, AB Variant D049290 - C18.452.648.595.554.825.300.300.920
└─└─└─└─└─└─└─└─

Rachitisme hypophosphatémique familial

Familial Hypophosphatemic Rickets D053098 - C18.654.521.500.133.770.734.875.500

Auteurs principaux

Guoyao Wu

6 publications dans cette catégorie

Affiliations :
  • Department of Animal Science, Texas A&M University, College Station, TX, 77843, USA. g-wu@tamu.edu.
Publications dans "Maladies métaboliques et nutritionnelles" : Voir toutes les publications (6)

Annabel Biruete

2 publications dans cette catégorie

Affiliations :
  • Department of Nutrition Science, Purdue University, West Lafayette, Indiana, USA, Division of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana.
Publications dans "Maladies métaboliques et nutritionnelles" :

Angela Yee-Moon Wang

2 publications dans cette catégorie

Affiliations :
  • Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.
Publications dans "Maladies métaboliques et nutritionnelles" :

Omar Ramos-Lopez

2 publications dans cette catégorie

Affiliations :
  • Medicine and Psychology School, Autonomous University of Baja California, Tijuana, Baja California, Mexico.
Publications dans "Maladies métaboliques et nutritionnelles" :

Shlomit Shalitin

2 publications dans cette catégorie

Publications dans "Maladies métaboliques et nutritionnelles" :

Cosimo Giannini

2 publications dans cette catégorie

Publications dans "Maladies métaboliques et nutritionnelles" :

Peng Li

2 publications dans cette catégorie

Affiliations :
  • North American Renderers Association, Alexandria, VA, 22314, USA.
Publications dans "Maladies métaboliques et nutritionnelles" :

Wenliang He

2 publications dans cette catégorie

Affiliations :
  • Department of Animal Science, Texas A&M University, College Station, TX, USA.
Publications dans "Maladies métaboliques et nutritionnelles" :

Marc A Benninga

2 publications dans cette catégorie

Affiliations :
  • Department of Pediatric Gastroenterology and Nutrition, Amsterdam University Medical Centers, Emma Children's Hospital, 1105 AZ Amsterdam, The Netherlands.
Publications dans "Maladies métaboliques et nutritionnelles" :

Wouter J de Jonge

2 publications dans cette catégorie

Affiliations :
  • Tytgat Institute for Liver and Intestinal Research, Amsterdam Gastroenterology and Metabolism, Academic Medical Center, University of Amsterdam, 1105 BK Amsterdam, The Netherlands.
  • Department of Surgery, University of Bonn, 53127 Bonn, Germany.
Publications dans "Maladies métaboliques et nutritionnelles" :

Gerardo Siani

1 publication dans cette catégorie

Affiliations :
  • DVM, 84133 Salerno, Italy.
Publications dans "Maladies métaboliques et nutritionnelles" :

Beatrice Mercaldo

1 publication dans cette catégorie

Affiliations :
  • Department of Veterinary Medicine and Animal Productions, University Federico II of Napoli, Via F. Delpino 1, 80137 Napoli, Italy.
Publications dans "Maladies métaboliques et nutritionnelles" :

Maria Chiara Alterisio

1 publication dans cette catégorie

Affiliations :
  • Department of Veterinary Medicine and Animal Productions, University Federico II of Napoli, Via F. Delpino 1, 80137 Napoli, Italy.
Publications dans "Maladies métaboliques et nutritionnelles" :

Antonio Di Loria

1 publication dans cette catégorie

Affiliations :
  • Department of Veterinary Medicine and Animal Productions, University Federico II of Napoli, Via F. Delpino 1, 80137 Napoli, Italy.
Publications dans "Maladies métaboliques et nutritionnelles" :

Adam J Rose

1 publication dans cette catégorie

Affiliations :
  • Nutrient Metabolism & Signalling Laboratory, Department of Biochemistry and Molecular Biology, Metabolism, Diabetes and Obesity Program, Biomedicine Discovery Institute, Monash University, Clayton 3800, Australia. adam.rose@monash.edu.
Publications dans "Maladies métaboliques et nutritionnelles" :

Aleksandra Mędza

1 publication dans cette catégorie

Affiliations :
  • Department of Pediatrics, Pediatric Gastroenterology, Allergology and Nutrition, Copernicus Hospital, Nowe Ogrody 1-6, 80-803 Gdansk, Poland.
Publications dans "Maladies métaboliques et nutritionnelles" :

Agnieszka Szlagatys-Sidorkiewicz

1 publication dans cette catégorie

Affiliations :
  • Department of Pediatrics, Pediatric Gastroenterology, Allergology and Nutrition, Medical University of Gdańsk, 80-210 Gdansk, Poland.
Publications dans "Maladies métaboliques et nutritionnelles" :

Yan He

1 publication dans cette catégorie

Affiliations :
  • College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
  • Engineering Research Center of Green Development for Conventional Aquatic Biological Industry in the Yangtze River Economic Belt, Ministry of Education, Wuhan 430070, China.
  • Key Lab of Freshwater Animal Breeding, Ministry of Agriculture and Rural Affair/Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Ministry of Education, Wuhan 430070, China.
Publications dans "Maladies métaboliques et nutritionnelles" :

Qingsong Tan

1 publication dans cette catégorie

Affiliations :
  • College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
  • Engineering Research Center of Green Development for Conventional Aquatic Biological Industry in the Yangtze River Economic Belt, Ministry of Education, Wuhan 430070, China.
  • Key Lab of Freshwater Animal Breeding, Ministry of Agriculture and Rural Affair/Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Ministry of Education, Wuhan 430070, China.
Publications dans "Maladies métaboliques et nutritionnelles" :

Qingchao Wang

1 publication dans cette catégorie

Affiliations :
  • College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
  • Engineering Research Center of Green Development for Conventional Aquatic Biological Industry in the Yangtze River Economic Belt, Ministry of Education, Wuhan 430070, China.
  • Key Lab of Freshwater Animal Breeding, Ministry of Agriculture and Rural Affair/Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Ministry of Education, Wuhan 430070, China.
Publications dans "Maladies métaboliques et nutritionnelles" :

Sources (10000 au total)

Contribution of Nutritional, Lifestyle, and Metabolic Risk Factors to Parkinson's Disease.

26 Mar 2024
DOI: 10.1002/mds.29778 PMID: 38532309

Modifiable risk factors for Parkinson's disease (PD) are poorly known.... The aim is to evaluate independent associations of different nutritional components, physical activity, and sedentary behavior and metabolic factors with the risk of PD.... In this population-based prospective cohort study using the data of the United Kingdom Biobank (from 2006-2010), 502,017 men and women who were free from PD (International Classification of Diseases 1... During a median follow-up of 12.8 years, lifestyle factors including vigorous physical activity (hazard ration [HR] = 0.84; 95% confidence interval [CI], 0.75-0.94), low-to-moderate sitting time (HR =... Vigorous physical activity, reduced sitting time, good sleep quality together with small coffee intake and vitamin D supplementation are potentially neuroprotective lifestyle interventions for the pre...