Global Variome shared LOVD

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Phenotype #0000232740 Individual ID 00306917 Associated disease CMT Phenotype details see paper; ..., first symptoms childhood/early adulthood, cramps lower limbs, distal lower limb weakness, sensory loss during initial examination, hand weakness appeared after distal lower limbs paresis Diagnosis/Initial Charcot-Marie-Tooth disease Inheritance Familial, autosomal dominant Diagnosis/Definite CMT2Z Age/Examination - 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 2020-07-24 08:48:44 +02:00 (CEST) Date last edited N/A

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