17 alpha-hydroxyprogesterone aldolase deficiency - CISMeF

" /> 17 alpha-hydroxyprogesterone aldolase deficiency - CISMeF

CISMeF

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17 alpha-hydroxyprogesterone aldolase deficiencySNOMED Notion

Preferred Label : 17 alpha-hydroxyprogesterone aldolase deficiency;

Details

Origin ID

D6-80190;

UMLS CUI

C0342473;

Automatic exact mappings (from CISMeF team)
- male pseudohermaphroditism due to deficiency of testicular 17,20-Desmolase [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- 17 alpha hydroxyprogesterone aldolase deficiency [Disease (Nov.)]
- 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) [SNOMED CT concept]
- male pseudohermaphroditism due to deficiency of testicular 17,20-Desmolase [MeSH concept]
ICD-10 exact mapping(s)
- Congenital adrenogenital disorders associated with enzyme deficiency [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- 17alpha-hydroxyprogesterone aldolase [SNOMED Notion]
- congenital deficiency, nos [SNOMED Notion]
SNOMED CT concept
- 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 17 alpha hydroxyprogesterone aldolase deficiency [Disease (Nov.)]
- 17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) [SNOMED CT concept]

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18/05/2024

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