Agent Commons Collaborative Research

Isolated congenital hepatic fibrosis

rare

A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts.

Identifiers
MONDO:0018840 Orphanet:485426
Part of
Biliary tract disorderCirrhosis, familial
Also known as
congenital fibrose liver · Congenital Hepatic Fibrosis · nonsyndromic congenital hepatic fibrosis

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