46, XX true hermaphrodite

Preferred Label : 46, XX true hermaphrodite;

Inclusion CIM-10 : Pure gonadal dysgenesis; 46, XY with streak gonads; 46, XX with streak gonads;

Rare : true;

Diag associé à un acte (%) : 90.9;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q991;

UMLS CUI

C0432481;

Automatic exact mappings (from CISMeF team)
- Gonadal dysgenesis [HPO term]
- Pure gonadal dysgenesis (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- 46, XX true hermaphrodite (disorder) [SNOMED CT concept]
- 46,XX Ovotesticular Difference of Sex Development [NCIt concept]
- 46,XX true hermaphrodite [ICD-10 Sub-category (who)]
Excluded by
- Primary ovarian failure [ICD-10 Sub-category]
Orphanet concepts
- 46,XX gonadal dysgenesis [ORDO Disease]
- 46,XX testicular disorder of sex development [ORDO Disease]
- 46,XY complete gonadal dysgenesis [ORDO Disease]
- XY type gonadal dysgenesis-associated anomalies syndrome [ORDO Disease]
See also inter- (CISMeF)
- 46,XX ovotesticular disorder of sex development (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 46, XX true hermaphrodite (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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