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 InternationalCreative Commons License
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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