Phenotype #0000166484

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	00218034
Associated disease	MYOP
Phenotype details	-
Diagnosis/Initial	congenital myopathy
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	CCD
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Tom Winder
Database submission license
Created by	Johan den Dunnen
Date created	2013-07-01 18:26:35 +02:00 (CEST)
Date last edited	N/A

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