Phenotype #0000125721

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Gajja Salomons and Eric Wever

Individual ID	00152986
Associated disease	CMS
Phenotype details	-
Diagnosis/Initial	syndrome, myasthenic, congenital, slow channel
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	1d
Phenotype/Onset	weak cry
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2011-02-13 11:28:19 +01:00 (CET)
Date last edited	2012-12-21 10:33:49 +01:00 (CET)

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