Disease #05338 (DFNA73 (deafness, autosomal dominant, type 73 (DFNA-73)), OMIM:617663)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	DFNA73
Name	deafness, autosomal dominant, type 73 (DFNA-73)
OMIM ID	617663
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PTPRQ
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-10-25 22:31:20 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.