 46, XX Disorders of Sex Development
"46, XX 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 with a female karyotype, in which the development of the gonadal or anatomical sex is atypical.
| Descriptor ID |
D058489
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| MeSH Number(s) |
C12.706.316.064 C13.351.875.253.064 C16.131.939.316.064 C19.391.119.064
|
| Concept/Terms |
Female Pseudohermaphroditism- Female Pseudohermaphroditism
- Female Pseudohermaphroditisms
- Pseudohermaphroditism, Female
- Pseudohermaphroditisms, Female
|
Below are MeSH descriptors whose meaning is more general than "46, XX Disorders of Sex Development".
Below are MeSH descriptors whose meaning is more specific than "46, XX Disorders of Sex Development".
This graph shows the total number of publications written about "46, XX Disorders of Sex Development" by people in this website by year, and whether "46, XX Disorders of Sex Development" was a major or minor topic of these publications.
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Below are the most recent publications written about "46, XX Disorders of Sex Development" by people in Profiles.
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Shoar Z, Ganguly T, Anderson CE, De Luca F, Suarez E. Absence of WNT4 gene mutation in a patient with MURCS association. J Pediatr Endocrinol Metab. 2014 May; 27(5-6):555-9.
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