fragile site 16p12

Preferred Label : fragile site 16p12;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565301;

UMLS CUI

C1850985;

Automatic exact mappings (from CISMeF team)
- Chromosome 16p12.1 deletion syndrome, 520-kb [OMIM Phenotype]
Related record
- fragile site 16p12 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]