Global Variome shared LOVD

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Phenotype #0000232748 Individual ID 00306925 Associated disease CMT Phenotype details see paper; ..., difficulty in run; distal leg atrophy; distal leg weakness; upper extremity involvement; no proximal involvement; no laterality; no cognitive impairment; tremor tongue atrophy Diagnosis/Initial Charcot-Marie-Tooth disease Inheritance Isolated (sporadic) Diagnosis/Definite CMT2Z Age/Examination 33y (33 years) Age/Diagnosis - Age/Onset 28y Phenotype/Onset difficulty in run Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-07-24 09:59:44 +02:00 (CEST) Date last edited N/A

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