PCDH15, protocadherin related 15, 65217

N. diseases: 94; N. variants: 122
Disease: Hearing Loss, Extreme ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme 		0.300 Biomarker phenotype CTD_human Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer. 10978835 2000