MeSH Browser

MeSH Supplementary: Polycystic liver disease
Unique ID: C536330
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536330
Entry Term(s): Isolated autosomal dominant polycystic liver disease; Isolated polycystic liver disease
Heading Mapped to: *Cysts; *Liver Diseases
Frequency: 344
Note: A predominantly autosomal dominant hereditary condition characterized by multiple cysts of various sizes in the LIVER of affected patients. May also occur together with AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE. Germline mutations in PRKCSH and SEC63 genes have been identified. OMIM: 174050
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Polycystic liver disease MeSH Supplementary Concept Data 2024