Disease #00294 (DFNB-86 (deafness, nonsyndromic, autosomal recessive, type 86 (DFNB-86)), OMIM:614617)

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Official abbreviation	DFNB-86
Name	deafness, nonsyndromic, autosomal recessive, type 86 (DFNB-86)
OMIM ID	614617
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBC1D24
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-01-08 19:33:40 +01:00 (CET)
Date last edited	N/A