COCH, cochlin, 1690

N. diseases: 45; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040264
Disease: Tinnitus
Tinnitus
0.110 GeneticVariation phenotype BEFREE Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus. 23374487 2013
CUI: C0040264
Disease: Tinnitus
Tinnitus
0.110 Biomarker phenotype HPO