Indeterminate sex and pseudohermaphroditism

Preferred Label : Indeterminate sex and pseudohermaphroditism;

ICD-10 exclusion note : pseudohermaphroditism with specified chromosomal anomaly (Q96-Q99); 46,XX true hermaphrodite (Q99.1); female pseudohermaphroditism with adrenocortical disorder (E25.-); pure gonadal dysgenesis (Q99.1); androgen insensitivity syndrome (E34.5-); chimera 46,XX/46,XY true hermaphrodite (Q99.0);

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Do not code with : true;

Détails

Origin ID

Q56;

UMLS CUI

C0021193;

Automatic exact mappings (from CISMeF team)
- Indeterminate sex and pseudohermaphroditism [ICD-9 code]
- Indeterminate sex and pseudohermaphroditism (disorder) [Inactive SNOMED CT concept]
- Malformative disorders of sex development [ICD-11 Category]
- pseudohermaphroditism [DO Concept]
DO Cross reference
- pseudohermaphroditism [DO Concept]
ICD-10 exclusion(s)
- Adrenogenital disorders [ICD-10 category]
- Androgen insensitivity syndrome [ICD-10 Sub-category]
- Other chromosome abnormalities, not elsewhere classified [ICD-10 category]
- Other sex chromosome abnormalities, female phenotype, not elsewhere classified [ICD-10 category]
- Other sex chromosome abnormalities, male phenotype, not elsewhere classified [ICD-10 category]
- Turner's syndrome [ICD-10 category]
Metaterm(s)
- gynecology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
- urology [CISMeF Metaterm]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Indeterminate sex and pseudohermaphroditism [ICD-9 code]
- Indeterminate sex and pseudohermaphroditism (disorder) [Inactive SNOMED CT concept]

Position du mot-clé dans l'(les) arborescence(s) :

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