Phenotype #0000001830

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00002674
Associated disease	CMYO6;MYPOP
Phenotype details	autosomal dominant inclusion body myopathy, joint contractures, ophthalmoplegia, rimmed vacuoles
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2013-09-19 18:49:34 +02:00 (CEST)
Date last edited	N/A

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