Disease #04466 (DFNB104 (deafness?, autosomal recessive, type 104 (DFNB104)), OMIM:616515)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DFNB104
Name	deafness?, autosomal recessive, type 104 (DFNB104)
OMIM ID	616515
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FAM65B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2020-06-29 13:36:13 +02:00 (CEST)

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