Phenotype #0000070217

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	00091907
Associated disease	BFH;TMN
Phenotype details	hearing loss
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Judy Savige
Database submission license	No license selected
Created by	Judy Savige
Date created	2011-08-10 05:54:23 +02:00 (CEST)
Date last edited	2016-12-16 13:01:26 +01:00 (CET)

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