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.

Follow this condition to get notified about new trials

Broader categories

Disease (717) Liver disorder (316) Hereditary disease (188) Digestive system disorder (166) Endocrine system disorder (78) Human disease (15) Hepatobiliary disorder (10) Autosomal dominant polycystic liver disease (3) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0)

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