Spinocerebellar ataxia

ICD-11 code : 8A03.16;

Preferred Label : Spinocerebellar ataxia;

Origin ID

600993818;

UMLS CUI

C0087012;

Automatic exact mappings (from CISMeF team)
- Ataxia [HPO term]
Currated CISMeF NLP mapping
- Autosomal dominant cerebellar ataxia [ORDO Disease]
- Spinocerebellar Ataxia [NCIt concept]
- Spinocerebellar ataxia [PASCAL descriptor]
- Spinocerebellar ataxia [MedDRA LLT]
- Spinocerebellar ataxia [OMIM phenotypic series]
- Spinocerebellar ataxia (disorder) [SNOMED CT concept]
- spinocerebellar ataxia [MedDRA Preferred Term]
- spinocerebellar ataxia [SNOMED Notion]
- spinocerebellar ataxia [Disease (Nov.)]
- spinocerebellar ataxias [MeSH Descriptor]
- spinocerebellar ataxias [MeSH concept]
ICD-10 Mapping
- Hereditary ataxia [ICD-10 category]
See also inter- (CISMeF)
- spinocerebellar degenerations [MeSH Descriptor]
- spinocerebellar degenerations [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant cerebellar ataxia [ORDO Disease]
- Spinocerebellar Ataxia [NCIt concept]
- Spinocerebellar ataxia [MedDRA LLT]
- Spinocerebellar ataxia (disorder) [SNOMED CT concept]
- Spinocerebellar atrophy [HPO term]
- autosomal dominant cerebellar ataxia [DO Concept]
- spinocerebellar ataxia [MedDRA Preferred Term]
- spinocerebellar ataxia [SNOMED Notion]
- spinocerebellar ataxias [MeSH Descriptor]
- spinocerebellar ataxias [MeSH concept]
Validated automatic mappings to BTNT
- Autosomal dominant cerebellar ataxia [ORDO Disease]
- autosomal dominant cerebellar ataxia [DO Concept]