Osebold skeletal dysplasia/osteolysis syndrome

Preferred Label : Osebold skeletal dysplasia/osteolysis syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 603389;

Details

Origin ID

603389;

UMLS CUI

C1863922;

Currated CISMeF NLP mapping
- osebold skeletal dysplasia osteolysis syndrome [MeSH concept]
- osebold skeletal dysplasia osteolysis syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- osebold skeletal dysplasia osteolysis syndrome [MeSH Supplementary Concept]
- osebold skeletal dysplasia osteolysis syndrome [MeSH concept]

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