Phenotype #0000162044

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	00213590
Associated disease	NEM
Phenotype details	-
Diagnosis/Initial	nemaline myopathy
Inheritance	Unknown
Diagnosis/Definite	NEM-1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Tom Winder
Database submission license
Created by	Johan den Dunnen
Date created	2012-10-19 16:27:59 +02:00 (CEST)
Date last edited	2012-10-23 21:20:17 +02:00 (CEST)

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