ring chromosomes

Preferred Label : ring chromosomes;

UMLS semantic type : T020 - Acquired Abnormality;

Origin ID

M0019123;

UMLS CUI

C0035639;

Automatic exact mappings (from CISMeF team)
- Ring chromosome Y syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Ring chromosome [ORDO Disease]
- Ring chromosome [MedDRA Preferred Term]
- Ring chromosome [PASCAL descriptor]
- Ring chromosome (disorder) [SNOMED CT concept]
- Ring chromosome (morphologic abnormality) [SNOMED CT concept]
- Supernumerary Circular Chromosome [NCIt concept]
- ring chromosome [SNOMED Notion]
Related record
- ring chromosomes [MeSH Descriptor]
Semantic type(s)
- Cell Component [UMLS semantic type]
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Ring chromosome [MedDRA Preferred Term]
- Ring chromosome (disorder) [SNOMED CT concept]
- Ring chromosome (morphologic abnormality) [SNOMED CT concept]
- Supernumerary Circular Chromosome [NCIt concept]
- ring chromosome [SNOMED Notion]
Validated automatic mappings to BTNT
- Ring chromosome Y [ICD-11 More detail]