Phenotype #0000243141

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	00324636
Associated disease	CMT
Phenotype details	see paper; ...
Diagnosis/Initial	Charcot-Marie-Tooth disease
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CMT2N
Age/Examination	26y (26 years)
Age/Diagnosis	-
Age/Onset	10y
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-12-20 16:14:59 +01:00 (CET)
Date last edited	N/A

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