pure gonadal dysgenesis 46,xx - CISMeF

" /> pure gonadal dysgenesis 46,xx - CISMeF

CISMeF

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Pure gonadal dysgenesis 46,xxSNOMED Notion

Preferred Label : pure gonadal dysgenesis 46,xx;

Détails

Origin ID

D4-80051;

UMLS CUI

C0685837;

Currated CISMeF NLP mapping
- 46 XX gonadal dysgenesis [DO Concept]
- 46,XX Gonadal Dysgenesis [NCIt concept]
- 46,XX gonadal dysgenesis [ICD-11 Subcategory]
- 46,XX gonadal dysgenesis [ORDO Disease]
- Ovarian dysgenesis 1 [OMIM Phenotype]
- Pure gonadal dysgenesis 46,XX (disorder) [SNOMED CT concept]
- gonadal dysgenesis, 46,XX [MeSH concept]
- gonadal dysgenesis, 46,xx [MeSH Descriptor]
- pure gonadal dysgenesis, 46, XX [MeSH concept]
ICD-10 exact mapping(s)
- Other congenital malformations of ovary [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Pure gonadal dysgenesis 46,XX (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Pure gonadal dysgenesis 46,XX (disorder) [SNOMED CT concept]
- pure gonadal dysgenesis, 46, XX [MeSH concept]

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28/07/2025

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