Alagille Syndrome


Alagille Syndrome 1

Alagille Syndrome 2

Alagille Watson Syndrome

Alagille's Syndrome

Alagille-Watson Syndrome

Alagilles Syndrome

Arteriohepatic Dysplasia

Arteriohepatic Dysplasia (AHD)

Cardiovertebral Syndrome

Cholestasis with Peripheral Pulmonary Stenosis

Ductular Hypoplasia, Hepatic

Dysplasia, Arteriohepatic

Dysplasia, Arteriohepatic (AHD)

Hepatic Ductular Hypoplasia

Hepatic Ductular Hypoplasia, Syndromatic

Hepatofacioneurocardiovertebral Syndrome

Hypoplasia, Hepatic Ductular

Paucity of Interlobular Bile Ducts

Syndrome, Alagille

Syndrome, Alagille Watson

Syndrome, Alagille's

Syndrome, Alagille-Watson

Syndrome, Cardiovertebral

Syndrome, Hepatofacioneurocardiovertebral

Syndrome, Watson Alagille

Syndrome, Watson Miller

Watson Alagille Syndrome

Watson Miller Syndrome

Watson-Miller syndrome

syndrome, Watson-Miller

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).