MeSH Browser

MeSH Supplementary: Persistent Mullerian duct syndrome
Unique ID: C536665
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536665
Entry Term(s): Hernia uteri inguinale; Persistent Muellerian duct syndrome; Persistent Mullerian Duct Syndrome, Types I And II; Persistent Müllerian Duct Syndrome; Persistent mullerian duct syndrome, types 1 and 2; Persistent oviduct syndrome; Pseudohermaphroditism, male internal
Registry Numbers: 0
Heading Mapped to: *Disorder of Sex Development, 46,XY
Frequency: 99
Note: An autosomal recessive congenital abnormality where mullerian derivatives, uterus and tubes, persist in otherwise normally virilized males. Mutations in the AMH gene and AMHR2 gene have been identified. OMIM: 261550
Date of Entry: 2010/08/25
Revision Date: 2018/01/12

Persistent Mullerian duct syndrome MeSH Supplementary Concept Data 2025