Phenotype #0000125769

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00153047
Associated disease	CMS
Phenotype details	phenotype compatible with adult onset SCCMS
Diagnosis/Initial	syndrome, myasthenic, congenital, slow channel (SCCMS)
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	73y (73 years)
Age/Diagnosis	-
Age/Onset	26y
Phenotype/Onset	-
Protein	-
Owner name	Angela Abicht
Database submission license	No license selected
Created by	Angela Abicht
Date created	2011-12-31 16:00:26 +01:00 (CET)
Date last edited	2012-03-04 15:56:04 +01:00 (CET)

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