Global Variome shared LOVD

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Phenotype #0000358106 Individual ID 00473311 Associated disease motor neuron disease Diagnosis/Initial motor neuron disease Diagnosis/Definite - Phenotype details Progressive lower and muscle weakness started 15y, bulbar dysfunction, dysphagia, dysarthria, achalasia, lower muscle atrophy, tongue weakness and atrophy, and motor neuron disease reported in EMG/NCV Inheritance Unknown Age/Examination 36y (36 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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