Multiple exostoses with spastic tetraparesis

Preferred Label : Multiple exostoses with spastic tetraparesis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant; possibly a contiguous gene syndrome;

Prefixed ID : 158345;

Details

Origin ID

158345;

UMLS CUI

C1834724;

Currated CISMeF NLP mapping
- multiple exostoses with spastic tetraparesis [MeSH concept]
- multiple exostoses with spastic tetraparesis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Multiple exostoses [HPO term]
- Spastic tetraparesis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- multiple exostoses with spastic tetraparesis [MeSH Supplementary Concept]
- multiple exostoses with spastic tetraparesis [MeSH concept]

Keyword's position in hierarchy(ies) :

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