Spinocerebellar ataxia type 18

Preferred Label : Spinocerebellar ataxia type 18;

ICD-11 definition : Spinocerebellar ataxia type 18 (SCA18) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by sensory neuropathy and cerebellar ataxia.;

Details

Origin ID

1564628854;

UMLS CUI

C1843884;

Currated CISMeF NLP mapping
- Sensorimotor neuropathy with ataxia, autosomal dominant [MeSH concept]
- Spinocerebellar ataxia 18 [OMIM Phenotype]
- Spinocerebellar ataxia type 18 [ORDO Disease]
- Spinocerebellar ataxia type 18 (disorder) [SNOMED CT concept]
- sensorimotor neuropathy with ataxia, autosomal dominant [MeSH Supplementary Concept]
- spinocerebellar ataxia 18 [Disease (Nov.)]
- spinocerebellar ataxia type 18 [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Sensorimotor neuropathy with ataxia, autosomal dominant [MeSH concept]
- Spinocerebellar ataxia 18 [OMIM Phenotype]
- Spinocerebellar ataxia type 18 [ORDO Disease]
- Spinocerebellar ataxia type 18 (disorder) [SNOMED CT concept]
- sensorimotor neuropathy with ataxia, autosomal dominant [MeSH Supplementary Concept]
- spinocerebellar ataxia 18 [Disease (Nov.)]
- spinocerebellar ataxia type 18 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients