Disease #02397 (DFNA-13 (deafness, autosomal dominant, type 13 (DFNA-13)), OMIM:601868)

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	Curator: Johan T. den Dunnen

Official abbreviation	DFNA-13
Name	deafness, autosomal dominant, type 13 (DFNA-13)
OMIM ID	601868
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL11A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A