Disease: Complete Hearing Loss ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss 		0.300 Biomarker phenotype CTD_human Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice. 15357422 2004