Anal sphincter myopathy, internal

Preferred Label : Anal sphincter myopathy, internal;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Proctalgia fugax due to anal sphincter myopathy;

Inheritance : Autosomal dominant;

Prefixed ID : 105565;

Details

Origin ID

105565;

UMLS CUI

C1862935;

Currated CISMeF NLP mapping
- anal sphincter myopathy, internal [MeSH concept]
- anal sphincter myopathy, internal [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the anus [HPO term]
- Autosomal dominant inheritance [HPO term]
- Constipation [HPO term]
- Myopathy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- anal sphincter myopathy, internal [MeSH Supplementary Concept]
- anal sphincter myopathy, internal [MeSH concept]

Keyword's position in hierarchy(ies) :

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