Phenotype #0000001758

Individual ID 00002844
Associated disease HMN5A
Phenotype details CMT2; CMT with and without pyramidal signs
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Onset -
Age/Examination -
Age/Diagnosis -
Protein -
Phenotype/Onset -
Owner name María-Jesús Sobrido
Database submission license No license selected
Created by María-Jesús Sobrido
Date created 2012-03-24 15:06:53 +01:00 (CET)
Date last edited N/A

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