Phenotypes for disease #00216 (SCA35 (ataxia, spinocerebellar, type 35 (SCA-35)), OMIM:613908)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000001867 HSP + Ataxia - - Familial, autosomal dominant - - - - - Marcel Nelen 00003016
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