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

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

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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)

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