XXYY Syndrome - CISMeF

Preferred Label : XXYY Syndrome;

NCIt synonyms : 48, XXYY Syndrome;

NCIt definition : A rare sex chromosome abnormality in which a male child has an extra X and Y chromosome.;

Details

Origin ID

C89801;

UMLS CUI

C2936741;

Currated CISMeF NLP mapping
- 48,XXYY Syndrome [MeSH concept]
- 48,XXYY syndrome [ORDO Disease]
- XXYY syndrome [MedDRA Preferred Term]
- XXYY syndrome (disorder) [SNOMED CT concept]
- klinefelter syndrome [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 48,XXYY Syndrome [MeSH concept]
- 48,XXYY syndrome [ORDO Disease]
- XXYY syndrome [MedDRA Preferred Term]
- XXYY syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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