Phenotype #0000046763

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	00059233
Associated disease	EDMD2;LGMD1B
Phenotype details	cardiac conduction defect
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Yulia Rogozhina
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2016-03-23 14:25:34 +01:00 (CET)
Date last edited	N/A

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