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, 0 tagged with Polycystic liver disease 4 with or without kidney cysts itself.

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↑ Autosomal dominant polycystic liver disease (3)

Including sub-types (0) Tagged with Polycystic liver disease 4 with or without kidney cysts (0)

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