spinocerebellar ataxia, autosomal recessive 3

Preferred Label : spinocerebellar ataxia, autosomal recessive 3;

Obsolete resource : true;

Approved symbol HGNC : SCAR3;

Chromosome HGNC : 6p23-p21;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:32976;

UMLS CUI

C1822621;

See also inter- (CISMeF)
- Spinocerebellar ataxia, autosomal recessive 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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