Phenotype #0000227511

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00300181
Associated disease	CMT2
Phenotype details	severe sensory and motor neuropathy, optic atrophy
Diagnosis/Initial	Charcot-Marie-Tooth disease, type 2
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CMT2A2
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-04-23 13:40:48 +02:00 (CEST)
Date last edited	N/A

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