radioulnar synostosis, radial ray abnormalities, and severe malformations in the male

Preferred Label : radioulnar synostosis, radial ray abnormalities, and severe malformations in the male;

Origin ID

C564557;

UMLS CUI

C1846147;

Automatic exact mappings (from CISMeF team)
- Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [OMIM Phenotype]
MeSH term(s) associated for indexing
- fingers [MeSH Descriptor]
- radius [MeSH Descriptor]
- synostosis [MeSH Descriptor]
- ulna [MeSH Descriptor]
Record concept(s)
- radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [OMIM Phenotype]