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Gonadal Dysgenesis, Mixed MeSH Descriptor Data 2022


MeSH Heading
Gonadal Dysgenesis, Mixed
Tree Number(s)
C12.050.351.875.253.309.391
C12.050.351.875.253.795.249
C12.200.706.316.309.391
C12.200.706.316.795.249
C12.800.316.309.391
C12.800.316.795.249
C16.131.260.830.835.249
C16.131.939.316.309.391
C16.131.939.316.795.249
C16.320.180.830.835.249
C19.391.119.309.391
C19.391.119.795.249
Unique ID
D006060
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006060
Scope Note
A type of defective gonadal development in patients with a wide spectrum of chromosomal mosaic variants. Their karyotypes are of partial sex chromosome monosomy resulting from an absence or an abnormal second sex chromosome (X or Y). Karyotypes include 45,X/46,XX; 45,X/46,XX/47,XXX; 46,XXp-; 45,X/46,XY; 45,X/47,XYY; 46,XYpi; etc. The spectrum of phenotypes may range from phenotypic female to phenotypic male including variations in gonads and internal and external genitalia, depending on the ratio in each gonad of 45,X primordial germ cells to those with normal 46,XX or 46,XY constitution.
Entry Term(s)
Mixed Gonadal Dysgenesis
Previous Indexing
Sex Differentiation Disorders (1966-1979)
Turner's Syndrome (1967-1979)
Public MeSH Note
91; was see under GONADAL DYSGENESIS 1980-90
History Note
91(80); was see under GONADAL DYSGENESIS 1980-90
Date Established
1991/01/01
Date of Entry
1978/12/21
Revision Date
2021/06/30
Gonadal Dysgenesis, Mixed Preferred
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