triple X syndrome

Preferred Label : triple X syndrome;

MeSH synonym : Triple-X chromosome syndrome; super female; XXX syndrome; Triple-X female; triplo X syndrome; 47,XXX syndrome; 47,Xxx; Trisomy X;

Details

Origin ID

C535318;

UMLS CUI

C0221033;

Currated CISMeF NLP mapping
- 47,XXX Syndrome [NCIt concept]
- Karyotype 47, XXX [ICD-10 Sub-category]
- Karyotype 47,XXX [ICD-11 Subcategory]
- Karyotype 47,XXX [ICD-10 Sub-category (who)]
- Trisomy X [NCIt concept]
- Trisomy X [ORDO Disease]
- Trisomy X syndrome (disorder) [SNOMED CT concept]
- XXX syndrome [MedDRA Preferred Term]
- trisomy x syndrome [SNOMED Notion]
MeSH term(s) associated for indexing
- chromosomes, human, X [MeSH Descriptor]
- sex chromosome aberrations [MeSH Descriptor]
- sex chromosome disorders of sex development [MeSH Descriptor]
- trisomy [MeSH Descriptor]
Record concept(s)
- Triple X syndrome [MeSH concept]
See also inter- (CISMeF)
- 47,XXX Karyotype [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 47,XXX Syndrome [NCIt concept]
- Karyotype 47, XXX [ICD-10 Sub-category]
- Karyotype 47,XXX [ICD-11 Subcategory]
- Trisomy X [ORDO Disease]
- Trisomy X [NCIt concept]
- Trisomy X syndrome (disorder) [SNOMED CT concept]
- XXX syndrome [MedDRA Preferred Term]
- trisomy x syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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