Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Alagille syndrome

MONDO:0007318

Alagille (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.

Also known as: Alagille syndrome, Alagille-Watson syndrome, Arteriohepatic dysplasia, syndromic bile duct paucity, Cardiovertebral syndrome, Hepatofacioneurocardiovertebral syndrome, Watson Alagille syndrome, Watson-Miller syndrome

15 clinical trials for this condition and its sub-types, 15 tagged with Alagille syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by