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polycystic liver disease
Pathology:
- presence of multiple liver cysts of biliary epithelial origin
Genetics:
- autosomal dominant
- associated with defects in SEC63 gene (autosomal dominant)
- associated with defects in PRKCSH
Differential diagnosis:
- may occur independently from autosomal dominant polycystic kidney disease which may also be associated with hepatic cysts
General
genetic disease of the liver
Database Correlations
OMIM 174050
References
OMIM :accession 174050