chromosome 21 monosomy

Preferred Label : chromosome 21 monosomy;

MeSH synonym : monosomy 21;

Origin ID

C537108;

UMLS CUI

C0795875;

CISMeF manual mappings
- Monosomy 21 [ORDO Disease]
- complete monosomy 21 syndrome [SNOMED Notion]
Currated CISMeF NLP mapping
- 21q deletion [ICD-11 More detail]
- Complete monosomy 21 syndrome (disorder) [SNOMED CT concept]
- Monosomy 21 [NCIt concept]
MeSH term(s) associated for indexing
- chromosomes, human, pair 21 [MeSH Descriptor]
- monosomy [MeSH Descriptor]
Record concept(s)
- Chromosome 21 monosomy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Monosomy 21 [NCIt concept]
- Monosomy 21 [ORDO Disease]