Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
0.100 Biomarker disease HPO
Entrez Id: 29
Gene Symbol: ABR
ABR
0.010 Biomarker disease BEFREE Ten patients had sensorineural hearing loss (38%), two patients had conductive hearing loss (7.7%), one patient had a mixed hearing loss (3.8%), and two patients had an as yet undefined hearing loss (ABR had not yet been performed at the time of this study) (7.7%). 21982076 2011
Entrez Id: 90
Gene Symbol: ACVR1
ACVR1
0.100 Biomarker disease HPO
Entrez Id: 9508
Gene Symbol: ADAMTS3
ADAMTS3
0.100 Biomarker disease HPO
Entrez Id: 60509
Gene Symbol: AGBL5
AGBL5
0.100 Biomarker disease HPO
Entrez Id: 54806
Gene Symbol: AHI1
AHI1
0.100 Biomarker disease HPO
Entrez Id: 196
Gene Symbol: AHR
AHR
0.100 Biomarker disease HPO
Entrez Id: 8092
Gene Symbol: ALX1
ALX1
0.100 Biomarker disease HPO
Entrez Id: 257
Gene Symbol: ALX3
ALX3
0.100 Biomarker disease HPO
Entrez Id: 139285
Gene Symbol: AMER1
AMER1
0.100 Biomarker disease HPO
Entrez Id: 286
Gene Symbol: ANK1
ANK1
0.010 GeneticVariation disease BEFREE Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. 20358596 2010
Entrez Id: 56172
Gene Symbol: ANKH
ANKH
0.110 GeneticVariation disease BEFREE Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. 20358596 2010
Entrez Id: 56172
Gene Symbol: ANKH
ANKH
0.110 Biomarker disease HPO
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11
0.100 CausalMutation disease CLINVAR
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11
0.100 GeneticVariation disease CLINVAR
Entrez Id: 10297
Gene Symbol: APC2
APC2
0.100 Biomarker disease HPO
Entrez Id: 9411
Gene Symbol: ARHGAP29
ARHGAP29
0.100 Biomarker disease HPO
Entrez Id: 23370
Gene Symbol: ARHGEF18
ARHGEF18
0.100 Biomarker disease HPO
Entrez Id: 23568
Gene Symbol: ARL2BP
ARL2BP
0.100 Biomarker disease HPO
Entrez Id: 403
Gene Symbol: ARL3
ARL3
0.100 Biomarker disease HPO
Entrez Id: 84100
Gene Symbol: ARL6
ARL6
0.100 Biomarker disease HPO
Entrez Id: 55130
Gene Symbol: ARMC4
ARMC4
0.100 Biomarker disease HPO
Entrez Id: 421
Gene Symbol: ARVCF
ARVCF
0.100 Biomarker disease HPO
Entrez Id: 80816
Gene Symbol: ASXL3
ASXL3
0.100 CausalMutation disease CLINVAR Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome. 27075689 2016
Entrez Id: 145173
Gene Symbol: B3GLCT
B3GLCT
0.100 Biomarker disease HPO