chromosome 21, uniparental disomy of

Preferred Label : chromosome 21, uniparental disomy of;

MeSH synonym : mosaic trisomy 21; uniparental disomy of 21;

Is substance : O;

Origin ID

C536794;

UMLS CUI

C2931324;

Currated CISMeF NLP mapping
- Uniparental disomy of chromosome 21 [ORDO Disease]
MeSH term(s) associated for indexing
- chromosomes, human, pair 21 [MeSH Descriptor]
- mosaicism [MeSH Descriptor]
- trisomy [MeSH Descriptor]
- uniparental disomy [MeSH Descriptor]
Record concept(s)
- Chromosome 21, uniparental disomy of [MeSH concept]
See also inter- (CISMeF)
- Maternal uniparental disomy of chromosome 21 [ORDO Disease]
- Paternal uniparental disomy of chromosome 21 [ORDO Disease]
- Trisomy 21 Mosaicism [NCIt concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Uniparental disomy of chromosome 21 [ORDO Disease]