Ophthalmoplegia, familial static

Preferred Label : Ophthalmoplegia, familial static;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : External ophthalmoplegia, nonprogressive, congenital hereditary;

Inheritance : Autosomal dominant;

Prefixed ID : %165000;

Details

Origin ID

165000;

UMLS CUI

C1833839;

Currated CISMeF NLP mapping
- ophthalmoplegia, familial static [MeSH concept]
- ophthalmoplegia, familial static [MeSH Supplementary Concept]
HPO term(s)
- Anisocoria [HPO term]
- Autosomal dominant inheritance [HPO term]
- Nystagmus [HPO term]
- Ophthalmoplegia [HPO term]
- Ptosis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ophthalmoplegia, familial static [MeSH Supplementary Concept]
- ophthalmoplegia, familial static [MeSH concept]

Keyword's position in hierarchy(ies) :

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