Phenotype #0000083982

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00106167
Associated disease	MYOP
Phenotype details	dominant congenital myopthy; patients show generalized proximal weakness in early childhood; non-progressive
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Kristen Nowak
Database submission license	No license selected
Created by	Kristen Nowak
Date created	2007-11-09 14:05:52 +01:00 (CET)
Date last edited	2012-03-04 15:55:43 +01:00 (CET)

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