Spinocerebellar ataxia

ICD-11 code : 8A03.16;

Preferred Label : Spinocerebellar ataxia;

ICD-11 definition : Autosomal dominantly inherited ataxias associated with over 37 gene loci that involve progressive degeneration of the cerebellum and spinocerebellar tracts of the spinal cord, presenting with characteristic sensory loss, diminished tendon reflexes, Romberg sign, and positive Babinski sign(s).;

Details

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]

Keyword's position in hierarchy(ies) :

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