Disease #02327 (DFNA6;DFNA14;DFNA38 (Deafness, autosomal dominant, type A6), OMIM:600965)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DFNA6;DFNA14;DFNA38
Name	Deafness, autosomal dominant, type A6
OMIM ID	600965
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WFS1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2025-05-18 11:38:57 +02:00 (CEST)

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