nystagmus 4, congenital, autosomal dominant

Preferred Label : nystagmus 4, congenital, autosomal dominant;

MeSH synonym : vestibulocerebellar disorder with predominant ocular signs;

Origin ID

C537856;

UMLS CUI

C1836383;

Currated CISMeF NLP mapping
- Spinocerebellar ataxia 27a [OMIM Phenotype]
MeSH term(s) associated for indexing
- nystagmus, congenital [MeSH Descriptor]
Record concept(s)
- Nystagmus 4, congenital, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 27 [OMIM Phenotype]
- Spinocerebellar ataxia 27a [OMIM Phenotype]
- Spinocerebellar ataxia type 27 [ICD-11 More detail]
- Spinocerebellar ataxia type 27 [ORDO Disease]
- Spinocerebellar ataxia type 27 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 27 [Disease (Nov.)]