Global Variome shared LOVD

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Phenotype #0000356942 Individual ID 00472134 Associated disease NBIA2B Phenotype details Neurodegeneration, Iron accumulation in brain, Progressive cerebellar ataxia, Tremor, Bradykinesia, Dysmetria, Axial hypotonia, Dysarthria, Gait ataxia, Rigidity, Akinesia, Cerebellar atrophy, Hyperreflexia Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination 17y (17 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2026-01-09 14:56:16 +01:00 (CET) Date last edited 2026-01-10 09:33:53 +01:00 (CET)

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