Disease #06991 (DFNA80 (deafness, autosomal dominant, type 80), OMIM:619274)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	DFNA80
Name	deafness, autosomal dominant, type 80
OMIM ID	619274
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GREB1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-12-31 12:22:06 +01:00 (CET)
Date last edited	N/A

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