Disease #05949 (DFNB57 (deafness, autosomal recessive, type 57 (DFNB57)), OMIM:618003)

Global Variome shared LOVD

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

	Curator: David Baux

Official abbreviation	DFNB57
Name	deafness, autosomal recessive, type 57 (DFNB57)
OMIM ID	618003
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDZD7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-06-22 16:46:51 +02:00 (CEST)
Date last edited	N/A

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