47,XYY Karyotype

Preferred Label : 47,XYY Karyotype;

NCIt synonyms : 47,XYY; XYY Karyotype;

NCIt related terms : 47XYY;

NCIt definition : An abnormal sex chromosome karyotype where the individual has one X chromosome and has two copies of the Y chromosome. The normal autosomal karyotype is present.;

NCI Metathesaurus CUI : CL1642751;

Details

Origin ID

C176782;

UMLS CUI

C0043379;

CISMeF manual mappings
- Karyotype 47,XYY [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Chromosome Y duplication [ICD-11 More detail]
- Karyotype 47, XYY [ICD-10 Sub-category]
- XYY karyotype [MeSH concept]
- xyy karyotype [MeSH Descriptor]
See also inter- (CISMeF)
- 47, XYY syndrome [MeSH concept]
- 47, XYY syndrome [MeSH Supplementary Concept]
- 47,XYY syndrome [ORDO Disease]
- Double Y syndrome (disorder) [SNOMED CT concept]
- Male with double or multiple Y [ICD-11 Subcategory]
- XYY syndrome [MedDRA Preferred Term]
- double y syndrome [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Karyotype 47, XYY [ICD-10 Sub-category]
- XYY karyotype [MeSH concept]
- xyy karyotype [MeSH Descriptor]
concept_is_in_subset
- GCT Authorized Value Terminology [NCIt concept]
- GCT Molecular Analysis Table [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients