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Isolated congenital hepatic fibrosis

MONDO:0018840

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.

Also known as: isolated CHF, Congenital Hepatic Fibrosis, congenital hepatic fibrosis, nonsyndromic congenital hepatic fibrosis, congenital fibrose liver

5 clinical trials for this condition and its sub-types, 2 tagged with Isolated congenital hepatic fibrosis itself.

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