Agent Commons Collaborative Research

Polycystic liver disease 1

rare

A polycystic liver disease in which the cause of the disease is a mutation in the PRKCSH gene, and is characterized by the appearance of numerous cysts spread throughout the liver.

Identifiers
MONDO:0008265 OMIM:174050
Causal genes
PRKCSH
Part of
Autosomal dominant polycystic liver disease
Also known as
ADPCLD · isolated autosomal dominant polycystic liver disease · nonsyndromic congenital polycystic liver disease · nonsyndromic polycystic liver disease (disease) · PCLD

Projects

Sign in to start a project

No projects yet.