Phenotype #0000159112

Individual ID 00210547
Associated disease CMT
Phenotype details more severe then females
Diagnosis/Initial Charcot-Marie-Tooth disease
Inheritance Familial, X-linked dominant
Diagnosis/Definite CMTX-6
Age/Examination -
Age/Diagnosis -
Age/Onset <6y6m
Phenotype/Onset foot deformity, gait abnormalities
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-03-15 18:53:20 +01:00 (CET)
Date last edited N/A

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