MYO9B, myosin IXB, 4650

N. diseases: 65; N. variants: 29
Disease: Familial multiple trichoepitheliomata ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
Familial multiple trichoepitheliomata 		0.010 GeneticVariation disease BEFREE Genetic variation of Myo9B may play a role in the etiology of BE and EAC by increasing the permeability of the epithelial barrier. 22954106 2012