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
06708 SCA44 Spinocerebellar ataxia 44 617691 AD - - GRM1 - -
03739 SCAR13 ataxia, spinocerebellar, autosomal recessive, type 13 (SCAR-13) 614831 AR - - GRM1 - -
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