All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06307 SCA48 ?Spinocerebellar ataxia 48 618093 AD - - STUB1 - -
04079 SCAR16 ataxia, spinocerebellar, autosomal recessive, type 16 (SCAR-16) 615768 AR 1 1 STUB1 - -
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