MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Congenital ear anomaly NOS (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		0.010 GeneticVariation group BEFREE The exact mechanism through which myoVIIA mutations result in these inner-ear anomalies is unknown. 15886106 2005