Disease: Bilateral Deafness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3665473
Disease: Bilateral Deafness
Bilateral Deafness 		0.300 Biomarker phenotype CTD_human Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice. 15357422 2004