Female pseudohermaphroditism, not elsewhere classified

Preferred Label : Female pseudohermaphroditism, not elsewhere classified;

Inclusion CIM-10 : Female pseudohermaphroditism NOS;

Rare : true;

Diag associé à un acte (%) : 100.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q562;

UMLS CUI

C0495579;

Currated CISMeF NLP mapping
- 46, XX disorders of sex development [MeSH Descriptor]
- 46,XX disorder of sex development [ORDO Disease]
- Female pseudohermaphroditism [MedDRA LLT]
- Female pseudohermaphroditism [HPO term]
- Female pseudohermaphroditism (disorder) [SNOMED CT concept]
- Female pseudohermaphroditism, not elsewhere classified [ICD-10 Sub-category (who)]
- Pseudohermaphroditism female [MedDRA Preferred Term]
- female pseudohermaphroditism [SNOMED Notion]
- female pseudohermaphroditism [MeSH concept]
- female pseudohermaphrotidism [Disease (Nov.)]
Manual NTBT mappings (CISMeF)
- 46,XX disorder of sex development induced by androgens excess [ORDO Disease]
- 46,XX disorder of sex development induced by maternal-derived androgen [ORDO Disease]
- Aromatase deficiency [ORDO Disease]
- Generalized glucocorticoid resistance syndrome [ORDO Disease]
Orphanet concepts
- 46,XX disorder of sex development [ORDO Disease]
- 46,XX disorder of sex development induced by endogenous maternal-derived androgen [ORDO Disease]
- 46,XX disorder of sex development induced by exogenous maternal-derived androgen [ORDO Disease]
- 46,XX disorder of sex development induced by maternal-derived androgen [ORDO Disease]
- 46,XX disorder of sex development-anorectal anomalies syndrome [ORDO Disease]
- 46,XX disorder of sex development-skeletal anomalies syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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