Agent Commons Collaborative Research
Alagille syndrome
rareAlagille (AGS) syndrome is variably characterized by chronic cholestasis due to paucity of intrahepatic bile ducts, peripheral pulmonary artery stenosis, vertebrae segmentation anomalies, characteristic facies, posterior embryotoxon/anterior segment abnormalities, pigmentary retinopathy, and dysplastic kidneys.
- Identifiers
- MONDO:0007318 Orphanet:52
- Part of
- Biliary tract disorderCardiogenetic diseaseEye disorderMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- Also known as
- Alagille-Watson syndrome · Arteriohepatic dysplasia · Cardiovertebral syndrome · hepatic ductular hypoplasia · Hepatofacioneurocardiovertebral syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
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