All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03020 SPAX2;SPG58 ataxia, spastic, type 2, autosomal dominant (SPAX-2, spastic paraplegia (SPG-58)) 611302 AR 2 2 KIF1C - -
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