NLM Logo

Turner Syndrome MeSH Descriptor Data 2022


MeSH Heading
Turner Syndrome
Tree Number(s)
C12.050.351.875.253.309.872
C12.050.351.875.253.795.750
C12.200.706.316.309.872
C12.200.706.316.795.750
C12.800.316.309.872
C12.800.316.795.750
C14.240.400.980
C14.280.400.980
C16.131.240.400.970
C16.131.260.830.835.750
C16.131.939.316.309.872
C16.131.939.316.795.750
C16.320.180.830.835.750
C19.391.119.309.872
C19.391.119.795.750
Unique ID
D014424
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D014424
Annotation
in females; TURNER SYNDROME, MALE see NOONAN SYNDROME is also available
Scope Note
A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant.
Entry Term(s)
Bonnevie-Ullrich Syndrome
Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, XO
Monosomy X
Status Bonnevie-Ullrich
Turner's Syndrome
Ullrich-Turner Syndrome
NLM Classification #
QS 677
See Also
Noonan Syndrome
Public MeSH Note
2002; see TURNER'S SYNDROME 1963-2001; for BONNEVIE-ULLRICH SYNDROME see SEX CHROMOSOME ABNORMALITIES 1997-2001, see BONNEVIE-ULLRICH SYNDROME 1963-1996
History Note
2002(1963); for BONNEVIE-ULLRICH SYNDROME use SEX CHROMOSOME ABNORMALITIES 1963-2001
Date Established
2002/01/01
Date of Entry
1999/01/01
Revision Date
2021/06/30
Turner Syndrome Preferred
Gonadal Dysgenesis, 45,X Related
Bonnevie-Ullrich Syndrome Related
page delivered in 0.166s