Disease #05410 (DFNB68 (deafness, autosomal recessive, type 68 (DFNB-68)), OMIM:610419)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DFNB68
Name	deafness, autosomal recessive, type 68 (DFNB-68)
OMIM ID	610419
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	S1PR2
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-03-23 10:53:33 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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