47,XXX Karyotype

Preferred Label : 47,XXX Karyotype;

NCIt synonyms : 47,XXX;

NCIt related terms : 47XXX;

NCIt definition : An abnormal sex chromosome karyotype where the individual has three copies of the X chromosome. The normal autosomal karyotype is present. This karyotype is associated with triple X syndrome.;

NCI Metathesaurus CUI : CL358890;

Détails

Origin ID

C176785;

UMLS CUI

C5444988;

Automatic exact mappings (from CISMeF team)
- Karyotype 47, XXX [ICD-10 Sub-category]
- Karyotype 47,XXX [ICD-11 Subcategory]
See also inter- (CISMeF)
- Trisomy X syndrome (disorder) [SNOMED CT concept]
- triple X syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Laboratory or Test Result [UMLS semantic type]
concept_is_in_subset
- GCT Authorized Value Terminology [NCIt concept]
- GCT Molecular Analysis Table [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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