Global Variome shared LOVD

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Phenotype #0000254575 Individual ID 00359279 Associated disease HMN Phenotype details see paper; ..., distal weakness LL; proximal weakness LL; spasticity lower legs; sensory involvement LL; pes cavus; no CNS involvement Diagnosis/Initial distal hereditary motor neuropathy Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 30y (30 years) Age/Diagnosis - Age/Onset - 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 2021-03-19 08:49:14 +01:00 (CET) Date last edited N/A

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