STRC, stereocilin, 161497

N. diseases: 25; N. variants: 12
Disease: Vertigo ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0042571
Disease: Vertigo
Vertigo 		0.110 GeneticVariation phenotype BEFREE Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype. 30250054 2018
CUI: C0042571
Disease: Vertigo
Vertigo 		0.110 CausalMutation phenotype CLINVAR