Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 10262
Gene Symbol: SF3B4
SF3B4
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 2706
Gene Symbol: GJB2
GJB2
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 91147
Gene Symbol: TMEM67
TMEM67
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 286002
Gene Symbol: SLC26A4-AS1
SLC26A4-AS1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 9786
Gene Symbol: KIAA0586
KIAA0586
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 27241
Gene Symbol: BBS9
BBS9
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 7399
Gene Symbol: USH2A
USH2A
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 8243
Gene Symbol: SMC1A
SMC1A
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 51651
Gene Symbol: PTRH2
PTRH2
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 117531
Gene Symbol: TMC1
TMC1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 CausalMutation CLINVAR

Entrez Id: 127343
Gene Symbol: DMBX1
DMBX1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR

Entrez Id: 5631
Gene Symbol: PRPS1
PRPS1
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
0.100 GeneticVariation CLINVAR