Global Variome shared LOVD

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Phenotype #0000358135 Individual ID 00473340 Associated disease paraplegia Diagnosis/Initial hereditary paraplegia Diagnosis/Definite - Phenotype details spastic gait, foot drop, corpus callosum hypoplasia, lower limb spasticity, mild muscle weakness, increased DTR, mild cognitive deficit and chronic inactive anterior horn cell disorder reported in EMG/NCV Inheritance Unknown Age/Examination 19y (19 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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