Phenotype #0000045632

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	00059043
Associated disease	DFNB;ARNSHL
Phenotype details	Congenital, profound, non-syndromic HL
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Zippi Brownstein
Database submission license
Created by	Zippi Brownstein
Date created	2016-02-18 23:51:46 +01:00 (CET)
Date last edited	2016-03-08 18:31:19 +01:00 (CET)

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