Polycystic liver disease 4 with or without kidney cysts

MONDO:0044327

An autosomal dominant disease characterized by adult-onset of liver cysts arising from the bile duct epithelium, caused by heterozygous mutation in the LRP5 gene. Some patients may develop a few kidney cysts, but these are often incidental and do not result in renal failure.

Also known as: polycystic liver disease 4 with or without kidney cysts, PCLD4

138 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by