Phenotype #0000058653

Individual ID 00078897
Associated disease CMT2
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 2y
Phenotype/Onset -
Protein -
Owner name Ki Wha Chung
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-05-14 17:17:39 +02:00 (CEST)
Date last edited N/A

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