chromosome 10, monosomy 10p

Preferred Label : chromosome 10, monosomy 10p;

UMLS semantic type : T049 - Cell or Molecular Dysfunction;

Origin ID

M0532749;

UMLS CUI

C0795836;

Related record
- 10p deletion syndrome (Partial) [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Partial deletion of the short arm of chromosome 10 [ORDO Disease]