Phenotype #0000127082

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	00111886
Associated disease	myotonia
Phenotype details	-
Diagnosis/Initial	myotonia congenita
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Becker disease
Age/Examination	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-02-23 17:58:57 +01:00 (CET)
Date last edited	2018-02-24 09:08:40 +01:00 (CET)

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