Global Variome shared LOVD

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Phenotype #0000292672 Individual ID 00399566 Associated disease CMTX1 Phenotype details see paper; ..., muscle weakness (HP:0001324); reduced tendon reflexes (HP:0001315); gait disturbance (HP:0001288); pes cavus (HP:0001761) Diagnosis/Initial CMT1X Inheritance Familial, X-linked Diagnosis/Definite - Age/Examination 65y (65 years) Age/Diagnosis - Age/Onset 35y Phenotype/Onset abnormal foot morphology (HP:0001760) Protein - Owner name Maeve Soen Database submission license Creative Commons Attribution 4.0 International Created by Maeve Soen Date created 2022-01-21 20:56:49 +01:00 (CET) Date last edited 2022-01-24 11:43:06 +01:00 (CET)

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