Global Variome shared LOVD

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Phenotype #0000358223 Individual ID 00473428 Associated disease paraplegia Diagnosis/Initial hereditary paraplegia Diagnosis/Definite - Phenotype details multiple affected siblings ,started 10y with gait abnormality, spastic gait, distal muscle weakness, pes cavus, impaierd heel-toe walking, hearing impairment since 44y , abnormal ABR and cental lesion suggested in EDX Inheritance Familial, autosomal recessive Age/Examination 54y (54 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - 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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