Disease #07048 (DFNB116 (deafness, autosomal recessive, type 116), OMIM:619093)

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	DFNB116
Name	deafness, autosomal recessive, type 116
OMIM ID	619093
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLDN9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-04 21:44:46 +01:00 (CET)
Date last edited	N/A

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