Spastic paraplegia with associated extrapyramidal signs

Preferred Label : Spastic paraplegia with associated extrapyramidal signs;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 182800;

Details

Origin ID

182800;

UMLS CUI

C1866852;

Currated CISMeF NLP mapping
- spastic paraplegia with associated extrapyramidal signs [MeSH concept]
- spastic paraplegia with associated extrapyramidal signs [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of extrapyramidal motor function [HPO term]
- Autosomal dominant inheritance [HPO term]
- Spastic paraplegia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- spastic paraplegia with associated extrapyramidal signs [MeSH Supplementary Concept]
- spastic paraplegia with associated extrapyramidal signs [MeSH concept]

Keyword's position in hierarchy(ies) :

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