Phenotype #0000125731

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Michel van Geel

Individual ID	00152997
Associated disease	CMS
Phenotype details	-
Diagnosis/Initial	syndrome, myasthenic, congenital, slow channel (SCCMS)
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Angela Abicht
Database submission license	No license selected
Created by	Angela Abicht
Date created	2011-12-28 11:54:56 +01:00 (CET)
Date last edited	2013-01-27 10:22:45 +01:00 (CET)

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