49,XXXXY Syndrome - CISMeF

CISMeF

chu

49,XXXXY SyndromeMeSH concept

Preferred Label : 49,XXXXY Syndrome;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Details

Origin ID

M0545763;

UMLS CUI

C0265499;

Currated CISMeF NLP mapping
- 49,XXXXY Syndrome [NCIt concept]
- 49,XXXXY syndrome [ORDO Disease]
- 49,XXXYY syndrome [ORDO Disease]
- 49,XXXYY syndrome (disorder) [SNOMED CT concept]
- 49,XYYYY syndrome [ORDO Disease]
- 49,XYYYY syndrome (disorder) [SNOMED CT concept]
- XXXXY syndrome (disorder) [SNOMED CT concept]
- xxxxy syndrome [SNOMED Notion]
Related record
- klinefelter syndrome [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 49,XXXXY Syndrome [NCIt concept]
- 49,XXXXY syndrome [ORDO Disease]
- XXXXY syndrome (disorder) [SNOMED CT concept]
- xxxxy syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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02/05/2025

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