Disease: Bell Palsy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376175
Disease: Bell Palsy
Bell Palsy 		0.020 GeneticVariation disease BEFREE The analysis of 29 cases with mutations of CHD7, the causative gene for CHARGE syndrome, clarified the relative importance of the cardinal features, including facial nerve palsy and facial asymmetry. 21338411 2011
CUI: C0376175
Disease: Bell Palsy
Bell Palsy 		0.020 GeneticVariation disease BEFREE We found that CHARGE individuals with CHD7 mutations more commonly have ocular colobomas, temporal bone anomalies (semicircular canal hypoplasia/dysplasia), and facial nerve paralysis compared with mutation negative individuals. 20186815 2010