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Up to: Autosomal dominant polycystic liver disease
Polycystic liver disease 4 with or without kidney cysts
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.
This condition has no sub-types.