Polyosteolysis-hyperostosis syndrome

Preferred Label : Polyosteolysis-hyperostosis syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 610830;

Details

Origin ID

610830;

UMLS CUI

C1835818;

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

Keyword's position in hierarchy(ies) :

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