fragile site 16p12

Preferred Label : fragile site 16p12;

MeSH note : deletion Chromomsome 16p12.1 Deletion Syndrome;

Origin ID

C565001;

UMLS CUI

C1850985;

Automatic exact mappings (from CISMeF team)
- Chromosome 16p12.1 deletion syndrome, 520-kb [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 16 [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- developmental disabilities [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
- mental disorders [MeSH Descriptor]
Record concept(s)
- fragile site 16p12 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]