Disease #00148 (DFNA17 (deafness, autosomal dominant, type 17 (DFNA-17)), OMIM:603622)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DFNA17
Name	deafness, autosomal dominant, type 17 (DFNA-17)
OMIM ID	603622
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH9
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2013-06-12 11:21:26 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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