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
04167 SCA ataxia, spinocerebellar (SCA) - - 194 189 FGF14, NOP56, NPTX1 - -
06984 SCA50 ataxia, spinocerebellar 620158 AD - - NPTX1 - -
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