Disease: Congenital deafness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		0.020 GeneticVariation disease BEFREE PMCA2 pump mutations and hereditary deafness. 29452611 2018
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		0.020 GeneticVariation disease BEFREE Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect. 22047666 2011