Phenotype #0000204016

Individual ID 00266240
Associated disease CMTX5
Phenotype details hearing loss, epilepsy, peripheral neuropathy, severe IUGR
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 00y06m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Laurence Jonard
Database submission license No license selected
Created by Laurence Jonard
Date created 2019-10-17 16:40:37 +02:00 (CEST)
Date last edited 2019-10-18 15:08:11 +02:00 (CEST)

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