Global Variome shared LOVD

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Phenotype #0000301382 Individual ID 00409265 Associated disease HMN Phenotype details see paper; ..., 10y-progressive weakness and muscle atrophy of the lower limbs Diagnosis/Initial distal hereditary motor neuropathy Inheritance Isolated (sporadic) Diagnosis/Definite HMN9 Age/Examination 35y (35 years) Age/Diagnosis - Age/Onset 10y 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 2022-05-06 10:30:52 +02:00 (CEST) Date last edited N/A

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