Spinocerebellar atrophy with pupillary paralysis

Preferred Label : Spinocerebellar atrophy with pupillary paralysis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 183100;

Details

Origin ID

183100;

UMLS CUI

C1866746;

Currated CISMeF NLP mapping
- spinocerebellar atrophy with pupillary paralysis [MeSH concept]
- spinocerebellar atrophy with pupillary paralysis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Spinocerebellar atrophy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- spinocerebellar atrophy with pupillary paralysis [MeSH Supplementary Concept]
- spinocerebellar atrophy with pupillary paralysis [MeSH concept]

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