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Alagille syndrome due to a JAG1 point mutation

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Uniprot Description A form of Alagille syndrome, an autosomal dominant multisystem disorder. It is clinically defined by hepatic bile duct paucity and cholestasis in association with cardiac, skeletal, and ophthalmologic manifestations. There are characteristic facial features and less frequent clinical involvement of the renal and vascular systems.
Mondo Term and Equivalent IDs
MONDO:0016862:  Alagille syndrome due to a JAG1 point mutation
Orphanet:261619: 
UMLS:C1956125: 
UMLS:CN202206: