Phenotype #0000153666

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00205495
Associated disease	CMT
Phenotype details	3-generation family, 3 affecteds
Diagnosis/Initial	Charcot-Marie-Tooth disease, type 2D (CMT-2D)
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CMT-2D
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2012-11-05 15:40:28 +01:00 (CET)
Date last edited	N/A

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