Polycystic liver disease 1

MONDO:0008265

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.

Also known as: isolated congenital polycystic liver disease, isolated polycystic liver disease, PCLD1, nonsyndromic congenital polycystic liver disease, nonsyndromic polycystic liver disease (disease), polycystic liver disease 1, polycystic liver disease 1 with or without kidney cysts, ADPCLD

0 clinical trials for this condition and its sub-types, 0 tagged with Polycystic liver disease 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant polycystic liver disease (3)

Including sub-types (0) Tagged with Polycystic liver disease 1 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.