Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0011053
Disease: Deafness
Deafness 		0.310 Biomarker CTD_human Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer. 10978835

2000
Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0011053
Disease: Deafness
Deafness 		0.310 GeneticVariation LHGDN To date, in our cohort of 557 Pakistani families, we have found 11 different PCDH15 mutations that account for deafness in 13 families. 18719945

2008