Global Variome shared LOVD

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Phenotype #0000356215 Individual ID 00471378 Associated disease DYT Diagnosis/Initial dystonia Diagnosis/Definite NEDISHM Phenotype details see paper; ..., combined dystonia, coexisting non-movement disorder-related neurological symptoms; onset infancy (0-2y); generalized dystonia; no dystonic cerebral palsy Inheritance Familial, autosomal recessive Age/Examination 08y (8 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 2025-12-19 18:53:19 +01:00 (CET) Date last edited 2026-03-08 10:22:00 +01:00 (CET)

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