Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.430 GeneticVariation CLINVAR

Entrez Id: 84059
Gene Symbol: ADGRV1
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 GeneticVariation CLINVAR

Entrez Id: 84059
Gene Symbol: ADGRV1
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 CausalMutation CLINVAR

Entrez Id: 7840
Gene Symbol: ALMS1
ALMS1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 GeneticVariation CLINVAR

Entrez Id: 9949
Gene Symbol: AMMECR1
AMMECR1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 25906
Gene Symbol: ANAPC15
ANAPC15
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 GeneticVariation CLINVAR

Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 171023
Gene Symbol: ASXL1
ASXL1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 414152
Gene Symbol: C10orf105
C10orf105
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.470 GeneticVariation CLINVAR

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.470 CausalMutation CLINVAR

Entrez Id: 23552
Gene Symbol: CDK20
CDK20
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 55636
Gene Symbol: CHD7
CHD7
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 CausalMutation CLINVAR

Entrez Id: 1159
Gene Symbol: CKMT1B
CKMT1B
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 GeneticVariation CLINVAR

Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.400 GeneticVariation CLINVAR

Entrez Id: 1280
Gene Symbol: COL2A1
COL2A1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.110 GeneticVariation CLINVAR

Entrez Id: 1286
Gene Symbol: COL4A4
COL4A4
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.110 GeneticVariation CLINVAR

Entrez Id: 1287
Gene Symbol: COL4A5
COL4A5
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.410 CausalMutation CLINVAR

Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome. 26612766

2016

Entrez Id: 22907
Gene Symbol: DHX30
DHX30
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 1834
Gene Symbol: DSPP
DSPP
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.400 GeneticVariation CLINVAR

Entrez Id: 1910
Gene Symbol: EDNRB
EDNRB
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 GeneticVariation CLINVAR

Entrez Id: 1910
Gene Symbol: EDNRB
EDNRB
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 CausalMutation CLINVAR

Entrez Id: 79813
Gene Symbol: EHMT1
EHMT1
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.100 GeneticVariation CLINVAR