Global Variome shared LOVD

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Phenotype #0000357952 Individual ID 00473157 Associated disease atrophy, cerebellar Diagnosis/Initial cerebellar atrophy Diagnosis/Definite - Phenotype details onset 55-56y , Gait ataxia; Cerebellar atrophy; Dysarthria; Impaired tandem gait; Hx. of ype I diabetes mellitus since 15y ago.Above clinical information is based on HPO nomenclature. Inheritance Familial, autosomal dominant Age/Examination 61y (61 years) Age/Diagnosis - Age/Onset - 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 2026-03-06 17:24:40 +01:00 (CET) Date last edited N/A

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