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Summary Literature (0)
MIM:215600 - CIRRHOSIS, FAMILIAL

Xenbase Genes: krt8.2, krt8, krt18, krt18.2, krt18.3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007329 - cirrhosis, familial
MONDO:0016204 - idiopathic copper-associated cirrhosis