Phenotype #0000162010

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	00213556
Associated disease	NEM
Phenotype details	mild, classical form
Diagnosis/Initial	nemaline myopathy
Inheritance	Familial
Diagnosis/Definite	NEM-1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2008-09-22 10:14:28 +02:00 (CEST)
Date last edited	2012-03-18 11:13:32 +01:00 (CET)

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