Phenotype #0000087606

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	00111805
Associated disease	myotonia congenita (AR)
Phenotype details	-
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	Thomsen disease
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2007-05-21 12:00:00 +02:00 (CEST)
Date last edited	2018-02-24 12:57:50 +01:00 (CET)

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