Amyotrophic dystonic paraplegia

Preferred Label : Amyotrophic dystonic paraplegia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 105300;

Details

Origin ID

105300;

UMLS CUI

C1862956;

Currated CISMeF NLP mapping
- amyotrophic dystonic paraplegia [MeSH concept]
- amyotrophic dystonic paraplegia [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bowel incontinence [HPO term]
- Dystonia [HPO term]
- Intellectual disability [HPO term]
- Nystagmus [HPO term]
- Skeletal muscle atrophy [HPO term]
- Spastic paraplegia [HPO term]
- Urinary incontinence [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- amyotrophic dystonic paraplegia [MeSH Supplementary Concept]
- amyotrophic dystonic paraplegia [MeSH concept]

Keyword's position in hierarchy(ies) :

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