spinocerebellar ataxia, autosomal recessive 6

Preferred Label : spinocerebellar ataxia, autosomal recessive 6;

MeSH synonym : norwegian infantile onset ataxia; cerebellar ataxia, infantile nonprogressive, autosomal recessive;

Details

Origin ID

C537312;

UMLS CUI

C1842676;

Currated CISMeF NLP mapping
- Infantile-onset autosomal recessive nonprogressive cerebellar ataxia [ORDO Disease]
- Spinocerebellar ataxia, autosomal recessive 6 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 6 [DO Concept]
DO Cross reference
- autosomal recessive spinocerebellar ataxia 6 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar degenerations [MeSH Descriptor]
Record concept(s)
- Spinocerebellar ataxia, autosomal recessive 6 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Infantile-onset autosomal recessive non progressive cerebellar ataxia (disorder) [SNOMED CT concept]
- Infantile-onset autosomal recessive nonprogressive cerebellar ataxia [ORDO Disease]
- Spinocerebellar ataxia, autosomal recessive 6 [OMIM Phenotype]
- autosomal recessive spinocerebellar ataxia 6 [DO Concept]

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