Phenotype #0000291679

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	00397527
Associated disease	CMT
Phenotype details	see paper ...
Diagnosis/Initial	Charcot-Marie-Tooth disease
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CMT1D
Age/Examination	24y (24 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Sarah El-Bestawi
Database submission license
Created by	Sarah El-Bestawi
Date created	2021-12-23 11:40:16 +01:00 (CET)
Date last edited	2022-01-06 14:26:15 +01:00 (CET)

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