Spinocerebellar ataxia type 23

Preferred Label : Spinocerebellar ataxia type 23;

ICD-11 definition : Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.;

Details

Origin ID

1340267869;

UMLS CUI

C1853250;

Currated CISMeF NLP mapping
- Spinocerebellar ataxia 23 [OMIM Phenotype]
- Spinocerebellar ataxia 23 [MeSH concept]
- Spinocerebellar ataxia type 23 [ORDO Disease]
- Spinocerebellar ataxia type 23 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 23 [MeSH Supplementary Concept]
- spinocerebellar ataxia 23 [Disease (Nov.)]
- spinocerebellar ataxia type 23 [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 23 [OMIM Phenotype]
- Spinocerebellar ataxia 23 [MeSH concept]
- Spinocerebellar ataxia type 23 [ORDO Disease]
- Spinocerebellar ataxia type 23 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 23 [MeSH Supplementary Concept]
- spinocerebellar ataxia 23 [Disease (Nov.)]
- spinocerebellar ataxia type 23 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients