Phenotype #0000207413

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00269609
Associated disease	DFNB32
Diagnosis/Initial	Non-syndromic hearing loss
Diagnosis/Definite	Non-syndromic hearing loss
Phenotype details	Congenital onset, severe-to-profound hearing loss
Inheritance	Familial, autosomal recessive
Age/Examination	43y (43 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Barbara Vona
Database submission license
Created by	Barbara Vona
Date created	2019-12-03 11:39:07 +01:00 (CET)
Date last edited	2019-12-04 11:06:06 +01:00 (CET)

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