All diseases

OMIM ID
215600
OMIM term:
CIRRHOSIS, FAMILIAL CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION, INCLUDED
Alternative terms:
INDIAN CHILDHOOD CIRRHOSIS, INCLUDED; ICC, INCLUDED
SEN SYNDROME, INCLUDED
COPPER-OVERLOAD CIRRHOSIS, INCLUDED
ENDEMIC TYROLEAN INFANTILE CIRRHOSIS, INCLUDED; ETIC, INCLUDED
COPPER TOXICOSIS, IDIOPATHIC, INCLUDED; ICT, INCLUDED
CIRRHOSIS, CRYPTOGENIC, INCLUDED
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO, INCLUDED
(∗) Location:
12q13.13  
(†) Associated OMIM genes:
KRT18   KRT8  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/m25vyxty