46, XX Testicular Disorders of Sex Development
"46, XX Testicular Disorders of Sex Development" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital conditions in individuals in which male GONADS develop in a genetic female (female to male sex reversal).
| Descriptor ID |
D058531
|
| MeSH Number(s) |
C12.706.316.064.124 C13.351.875.253.064.124 C16.131.939.316.064.124 C19.391.119.064.124
|
| Concept/Terms |
46, XX Testicular Disorders of Sex Development- 46, XX Testicular Disorders of Sex Development
- 46, XX Testicular Disorder of Sex Development
- XX Male Syndrome
- Syndrome, XX Male
- Syndromes, XX Male
- XX Male Syndromes
- 46, XX Testicular DSD
- XX Sex Reversal
- Reversal, XX Sex
- Reversals, XX Sex
- Sex Reversal, XX
- Sex Reversals, XX
- XX Sex Reversals
|
Below are MeSH descriptors whose meaning is more general than "46, XX Testicular Disorders of Sex Development".
- Diseases [C]
- Male Urogenital Diseases [C12]
- Urogenital Abnormalities [C12.706]
- Disorders of Sex Development [C12.706.316]
- 46, XX Disorders of Sex Development [C12.706.316.064]
- 46, XX Testicular Disorders of Sex Development [C12.706.316.064.124]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urogenital Abnormalities [C13.351.875]
- Disorders of Sex Development [C13.351.875.253]
- 46, XX Disorders of Sex Development [C13.351.875.253.064]
- 46, XX Testicular Disorders of Sex Development [C13.351.875.253.064.124]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Urogenital Abnormalities [C16.131.939]
- Disorders of Sex Development [C16.131.939.316]
- 46, XX Disorders of Sex Development [C16.131.939.316.064]
- 46, XX Testicular Disorders of Sex Development [C16.131.939.316.064.124]
- Endocrine System Diseases [C19]
- Gonadal Disorders [C19.391]
- Disorders of Sex Development [C19.391.119]
- 46, XX Disorders of Sex Development [C19.391.119.064]
- 46, XX Testicular Disorders of Sex Development [C19.391.119.064.124]
Below are MeSH descriptors whose meaning is more specific than "46, XX Testicular Disorders of Sex Development".
This graph shows the total number of publications written about "46, XX Testicular Disorders of Sex Development" by people in this website by year, and whether "46, XX Testicular Disorders of Sex Development" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "46, XX Testicular Disorders of Sex Development" by people in Profiles.
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Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (WT1) gene. Proc Natl Acad Sci U S A. 2020 06 16; 117(24):13680-13688.
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Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region. J Med Genet. 2017 10; 54(10):705-709.
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22q11.2q13 duplication including SOX10 causes sex-reversal and peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease. Am J Med Genet A. 2017 Apr; 173(4):1066-1070.