Subtype of: Deafness · Deafness, autosomal recessive

Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
Deafness, autosomal recessive, 4	MONDO_0010933	SLC26A4	Unknown	10700480 14679580 14508505 9500541 20108392 11748854 24051746 19204907 10190331 12676893 28281779 20597900 11919333 11932316 15689455 12974744 9618166 10602116 15355436 9618167 11317356 15531480	Open Targets	Thyroid hormone synthesis Multifunctional anion exchangers Defective SLC26A4 causes Pendred syndrome (PDS)

Deafness, autosomal recessive, 4