Phenotype #0000084252

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	00106448
Associated disease	MYOP
Phenotype details	myopathy, congenital
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Tom Winder
Database submission license	No license selected
Created by	Tom Winder
Date created	2011-10-04 17:29:56 +02:00 (CEST)
Date last edited	2012-03-09 19:12:55 +01:00 (CET)

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