Phenotype #0000287567

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Gerard Pals, Sonna Stolk, Raymond Dalgleish, and Dimitra Micha

Individual ID	00394363
Associated disease	-
Phenotype details	CMT with optic nerve changes, normal electroretinogram but flat flash VEP
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	Charcot-Marie-Tooth disease
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-12-01 10:17:04 +01:00 (CET)
Date last edited	N/A

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