47, XYY syndrome

Preferred Label : 47, XYY syndrome;

MeSH synonym : YY syndrome; XYY syndrome; 47 XYY syndrome; jacob's syndrome;

Origin ID

C535317;

UMLS CUI

C3266843;

Automatic exact mappings (from CISMeF team)
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [OMIM Phenotype]
Currated CISMeF NLP mapping
- 47,XYY Syndrome [NCIt 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]
False automatic mappings
- Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) [SNOMED CT concept]
- Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome [ORDO Disease]
- camptodactyly-arthropathy-coxa vara-pericarditis syndrome [DO Concept]
MeSH term(s) associated for indexing
- sex chromosome disorders [MeSH Descriptor]
- xyy karyotype [MeSH Descriptor]
ORDO relation(s)
- 47,XYY syndrome [ORDO Disease]
Record concept(s)
- 47, XYY syndrome [MeSH concept]
See also inter- (CISMeF)
- 47,XYY Karyotype [NCIt concept]
- Karyotype 47,XYY [ICD-10 Sub-category (who)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 47,XYY Syndrome [NCIt 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]