Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Término preferido
Alagille Syndrome
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Tipo
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mesh:Descriptor
Definición
- A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2).
Concepto genérico
Etiquetas alternativas
- Alagille Watson Syndrome
- Alagille's Syndrome
- Alagille-Watson Syndrome
- Arteriohepatic Dysplasia
- Arteriohepatic Dysplasia (AHD)
- Cardiovertebral Syndrome
- Cholestasis with Peripheral Pulmonary Stenosis
- Dysplasia, Arteriohepatic
- Hepatic Ductular Hypoplasia, Syndromatic
- Hepatofacioneurocardiovertebral Syndrome
- Watson Alagille Syndrome
- Watson Miller Syndrome
- Watson-Miller syndrome
En otras lenguas
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francés
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Cholestase avec sténose périphérique des branches de l'artère pulmonaire
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Dysplasie artério-hépatique
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Dysplasie artériohépatique
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Paucité des voies biliaires syndromique
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Paucité ductulaire syndromatique
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SAG (Syndrome d'AlaGille)
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Syndrome d'Alagille-Watson
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Syndrome de Watson-Alagille
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Syndrome de Watson-Miller
URI
http://data.loterre.fr/ark:/67375/JVR-K4CNPPTJ-D
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