Phenotype #0000125734

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	00153006
Associated disease	CMS
Phenotype details	-
Diagnosis/Initial	syndrome, myasthenic, congenital, slow channel
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
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 14:08:54 +01:00 (CET)
Date last edited	2022-07-07 16:00:25 +02:00 (CEST)

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