Phenotype #0000155122

Individual ID 00207340
Associated disease CMTX5
Phenotype details sensori-motor neuropathy since the age of 8
profound bilateral hearing loss
bilateral optic neuropathy
Diagnosis/Initial -
Inheritance Familial, X-linked
Diagnosis/Definite -
Age/Examination 35y (35 years)
Age/Diagnosis 35y
Age/Onset 08y
Phenotype/Onset 15y
Protein -
Owner name Justine Lerat
Database submission license No license selected
Created by Justine Lerat
Date created 2018-11-20 01:12:27 +01:00 (CET)
Date last edited 2018-11-20 19:53:25 +01:00 (CET)

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