Phenotype #0000046746

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	00060257
Associated disease	DFNA12
Phenotype details	Congenital, progressive, severe-profound NSHL
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Zippi Brownstein
Database submission license
Created by	Zippi Brownstein
Date created	2016-03-22 11:59:20 +01:00 (CET)
Date last edited	2016-03-28 10:46:58 +02:00 (CEST)

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