Trisomy 11 - CISMeF

Preferred Label : Trisomy 11;

NCIt definition : The presence of a third copy of chromosome 11 in somatic cells.;

Origin ID

C37191;

UMLS CUI

C0432409;

Automatic exact mappings (from CISMeF team)
- Trisomy 11 (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Trisomy 11 [MedDRA Preferred Term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Trisomy 11 [MedDRA Preferred Term]
- Trisomy 11 (disorder) [SNOMED CT concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Infantile Fibrosarcoma [NCIt concept]