Global Variome shared LOVD

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Phenotype #0000129342 Individual ID 00164232 Associated disease atrophy, cerebellar Diagnosis/Initial - Diagnosis/Definite - Phenotype details see paper; ..., cerebellar atrophy, spinal motor neuronopathy Inheritance Familial, autosomal recessive Age/Examination 02y04m (2 years, 4 months) Age/Diagnosis - Age/Onset 00y08m 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 2018-05-11 14:23:00 +02:00 (CEST) Date last edited N/A

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