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
04201 SCAR ataxia, spinocerebellar, autosomal recessive - AR 57 57 TDP2, VWA3B - -
05518 SCAR22 ataxia, spinocerebellar, autosomal recessive, type 22 (SCAR22) - AR - - VWA3B - -
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