MeSH Browser

MeSH Supplementary: 46,Xx Gonadal Dysgenesis, Partial Or Complete, Autosomal
Unique ID: C567597
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567597
Entry Term(s): Xx Male Syndrome, Sry-Negative
Registry Numbers: 0
Heading Mapped to: *Gonadal Dysgenesis, 46,XX
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

46,Xx Gonadal Dysgenesis, Partial Or Complete, Autosomal MeSH Supplementary Concept Data 2025