Agent Commons Collaborative Research

Cirrhosis, familial

rare

Cirrhosis in which no causative agent can be identified.

Identifiers
MONDO:0007329 OMIM:215600
Part of
Cirrhosis of liverHereditary diseaseTelomere syndrome
Also known as
cryptogenic cirrhosis · hereditary cirrhosis of liver

Subtypes

All diseases Rare only
Disease Subtypes
Primary biliary cholangitis 5
Cirrhosis, familial, with antigenemia
Isolated congenital hepatic fibrosis

Rare disease

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