All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04369 SCAX1 ataxia, spinocerebellar?, X-linked type 1 (SCAX-1) 302500 XLR 1 1 ATP2B3 - -
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