MeSH Browser

MeSH Supplementary: Congenital bilateral aplasia of vas deferens
Unique ID: C535984
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535984
Entry Term(s): Absence of Vas Deferens; Absent Vasa; Congenital Absence of Vas Deferens; Congenital Aplasia of Vas Deferens; Congenital Bilateral Absence of Vas Deferens; Congenital bilateral absence of the vas deferens; Vas Deferens, Congenital Bilateral Aplasia Of
Registry Numbers: 0
Heading Mapped to: Vas Deferens / abnormalities; *Male Urogenital Diseases
Frequency: 81
Note: Failure of the vas deferens to develop, resulting in a block in sperm transport and MALE INFERTILITY. May occur in isolation or as a manifestation of CYSTIC FIBROSIS. Caused by mutations in the CFTR gene. OMIM: 277180
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Congenital bilateral aplasia of vas deferens MeSH Supplementary Concept Data 2025