Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000138575 Individual ID 00168057 Associated disease ataxia Diagnosis/Initial Cerebellar Ataxia Diagnosis/Definite - Phenotype details Mild cerebellar atrophy, Dysarthria, UL & LL ataxia Inheritance Familial, autosomal recessive Age/Examination - Age/Onset 28y Phenotype/Onset - Protein - Owner name Inge Meijer Database submission license No license selected Created by Inge Meijer Date created 2018-07-27 18:36:13 +02:00 (CEST) Date last edited N/A

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