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

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 300233;

Details

Origin ID

300233;

UMLS CUI

C1846147;

Automatic exact mappings (from CISMeF team)
- radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [MeSH concept]
- radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [MeSH Supplementary 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 [MeSH Supplementary Concept]
- radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [MeSH concept]

Keyword's position in hierarchy(ies) :

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