Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7287
Gene Symbol: TULP1
TULP1
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 CausalMutation CLINVAR Antioxidant effect of aqueous extract of four plants with therapeutic potential on gynecological diseases; Semen persicae, Leonurus cardiaca, Hedyotis diffusa, and Curcuma zedoaria. 29178942

2017

Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 6295
Gene Symbol: SAG
SAG
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 2652
Gene Symbol: OPN1MW
OPN1MW
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 63916
Gene Symbol: ELMO2
ELMO2
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 79797
Gene Symbol: ZNF408
ZNF408
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 3030
Gene Symbol: HADHA
HADHA
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 9990
Gene Symbol: SLC12A6
SLC12A6
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 6023
Gene Symbol: RMRP
RMRP
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 27031
Gene Symbol: NPHP3
NPHP3
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 1001
Gene Symbol: CDH3
CDH3
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 10594
Gene Symbol: PRPF8
PRPF8
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 22926
Gene Symbol: ATF6
ATF6
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 3419
Gene Symbol: IDH3A
IDH3A
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 80184
Gene Symbol: CEP290
CEP290
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 CausalMutation CLINVAR

Entrez Id: 3052
Gene Symbol: HCCS
HCCS
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 57724
Gene Symbol: EPG5
EPG5
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 8481
Gene Symbol: OFD1
OFD1
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 25782
Gene Symbol: RAB3GAP2
RAB3GAP2
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 55975
Gene Symbol: KLHL7
KLHL7
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO

Entrez Id: 3423
Gene Symbol: IDS
IDS
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
0.100 Biomarker HPO