MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Linear atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		0.010 AlteredExpression disease BEFREE Myo7a and Kcnj10 expression analysis show a lack of the melanocyte-like intermediate cells in hb/hb stria vascularis, which can explain the absence of endocochlear potential. 23457544 2013