Global Variome shared LOVD

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Phenotype #0000157236 Individual ID 00208606 Associated disease SCA Phenotype details moderate ataxia, mild dysarthria, moderate down-beat nystagmus, diabetes mellitus; phenotype not more severe compared to heterozygous cases Diagnosis/Initial spinocerebellar ataxia Inheritance Familial, autosomal dominant Diagnosis/Definite SCA-6 Age/Examination 63y (63 years) Age/Diagnosis - Age/Onset 60y Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-12-11 21:54:04 +01:00 (CET) Date last edited 2018-12-11 21:57:37 +01:00 (CET)

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