adrenogenital syndrome

Preferred Label : adrenogenital syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0000488;

UMLS CUI

C0302280;

Automatic exact mappings (from CISMeF team)
- Adrenogenital disorder, unspecified [ICD-10 Sub-category (who)]
- Adrenogenital syndrome [ACR pathology]
- Adrenogenital syndrome [ACR pathology]
Currated CISMeF NLP mapping
- Adrenogenital Syndrome [NCIt concept]
- Adrenogenital disorder (disorder) [SNOMED CT concept]
- Adrenogenital disorders [ICD-11 Category]
- Adrenogenital syndrome [PASCAL descriptor]
- Adrenogenital syndrome [MedDRA Preferred Term]
- Adrenogenital syndrome [HPO term]
- Adrenogenital syndrome [ORDO Disease]
- Adrenogenital syndrome NOS [MedDRA LLT]
- Congenital Adrenal Hyperplasia [NCIt concept]
- adrenogenital syndrome [Disease (Nov.)]
- congenital adrenal cortical hyperplasia, nos [SNOMED Notion]
Related record
- adrenogenital syndrome [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ADRENOGENITAL SYNDROME CONGENITAL [WHO-ART Preferred Term]
- Adrenal virilism [MedDRA LLT]
- Adrenal virilism (disorder) [SNOMED CT concept]
- Adrenogenital Syndrome [NCIt concept]
- Adrenogenital syndrome [MedDRA Preferred Term]
- Adrenogenital syndrome [HPO term]
- Adrenogenital syndrome NOS [MedDRA LLT]
- Adrenogenital syndrome congenital [MedDRA LLT]
- Androgenital syndrome [MedDRA LLT]
- Congenital adrenogenital syndrome (disorder) [Inactive SNOMED CT concept]
- congenital adrenal cortical hyperplasia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- congenital adrenal hyperplasia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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