SLC26A4, solute carrier family 26 member 4, 5172

N. diseases: 194; N. variants: 174
Disease: Vertigo ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0042571
Disease: Vertigo
Vertigo 		0.120 GeneticVariation phenotype BEFREE Clinical characteristics of patients with SLC26A4 mutations were congenital, fluctuating and progressive hearing loss usually associated with vertigo and/or goiter. 24599119 2014
CUI: C0042571
Disease: Vertigo
Vertigo 		0.120 GeneticVariation phenotype BEFREE The present study confirmed the clinical characteristics of patients with SLC26A4 mutations: congenital, fluctuating, and progressive hearing loss usually associated with vertigo and/or goiter during long-term follow-up. 17851929 2007
CUI: C0042571
Disease: Vertigo
Vertigo 		0.120 Biomarker phenotype HPO