MeSH Browser

MeSH Supplementary: Prostate cancer, familial
Unique ID: C537243
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537243
Entry Term(s): Hereditary prostate cancer; Prostate Cancer, Hereditary, 1
Registry Numbers: 0
Heading Mapped to: *Prostatic Neoplasms
Frequency: 70
Note: Germline mutations in the RNASEL gene have been identified for an autosomal dominant form of hereditary prostate cancer (OMIM: 601518). Several other loci which confer susceptibility to prostate cancer have also been mapped. OMIM: 176807
Date of Entry: 2010/08/25
Revision Date: 2019/05/17

Prostate cancer, familial MeSH Supplementary Concept Data 2025