Phenotype #0000160403

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	00211922
Associated disease	CNM
Phenotype details	severe (at birth)
Diagnosis/Initial	myotubular myopathy
Inheritance	Isolated (sporadic)
Diagnosis/Definite	CNMX
Age/Examination	-
Age/Diagnosis	-
Age/Onset	0d
Phenotype/Onset	-
Protein	-
Owner name	Wolfram Kress
Database submission license
Created by	Johan den Dunnen
Date created	2012-01-16 20:30:45 +01:00 (CET)
Date last edited	2012-07-10 15:12:30 +02:00 (CEST)

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