All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04669 SCAR20 ataxia, spinocerebellar, autosomal recessive, type 20 (SCAR-20) 616354 AR 3 3 SNX14 - -
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