OTOGL, otogelin like, 283310

N. diseases: 9; N. variants: 8
Disease: hearing impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.120 GeneticVariation phenotype BEFREE Defects in either cause the DFNB18B and DFNB84B genetic forms of deafness, respectively, both characterized by congenital mild-to-moderate hearing impairment. 31776257 2019
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.120 GeneticVariation phenotype BEFREE Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. 23850727 2013
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.120 GeneticVariation phenotype CLINVAR
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.120 Biomarker phenotype HPO