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
06331 SCA42 Spinocerebellar ataxia 42 616795 AD - - CACNA1G - -
06357 SCA42ND Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits 618087 AD - - CACNA1G - -
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