deafness, congenital heart defects, and posterior embryotoxon

Preferred Label : deafness, congenital heart defects, and posterior embryotoxon;

Origin ID

C566604;

UMLS CUI

C1866053;

Automatic exact mappings (from CISMeF team)
- Deafness, congenital heart defects, and posterior embryotoxon [OMIM Phenotype]
MeSH term(s) associated for indexing
- cornea [MeSH Descriptor]
- hearing loss [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
Record concept(s)
- deafness, congenital heart defects, and posterior embryotoxon [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, congenital heart defects, and posterior embryotoxon [OMIM Phenotype]