Phenotype #0000155396

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00207585
Associated disease	CMT
Phenotype details	sensori-motor demyelinating neuropathy and severe auditory neuropathy
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	33y (33 years)
Age/Diagnosis	-
Age/Onset	05y
Phenotype/Onset	20y
Protein	MYH14
Owner name	Justine Lerat
Database submission license	No license selected
Created by	Justine Lerat
Date created	2018-11-25 18:30:16 +01:00 (CET)
Date last edited	2018-12-03 15:40:50 +01:00 (CET)

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