Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:215600 - CIRRHOSIS, FAMILIAL

Xenbase Genes: krt8.2, krt8.1, krt18.1, krt18.2, krt18.3

Human Disease Resource: OMIM

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