Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112476
Gene Symbol: PRRT2
PRRT2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.500 Biomarker HPO

Entrez Id: 2775
Gene Symbol: GNAO1
GNAO1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.500 GeneticVariation CLINVAR

Entrez Id: 3064
Gene Symbol: HTT
HTT
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.440 Biomarker HPO

Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.410 Biomarker HPO

Entrez Id: 200424
Gene Symbol: TET3
TET3
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.300 Biomarker GENOMICS_ENGLAND

Entrez Id: 1949
Gene Symbol: EFNB3
EFNB3
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.200 Biomarker MGD

Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.200 Biomarker HPO

Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.150 Biomarker HPO

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 Biomarker HPO

Entrez Id: 23221
Gene Symbol: RHOBTB2
RHOBTB2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR

Entrez Id: 2629
Gene Symbol: GBA
GBA
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 SusceptibilityMutation CLINVAR

Entrez Id: 11212
Gene Symbol: PLPBP
PLPBP
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 Biomarker HPO

Entrez Id: 6812
Gene Symbol: STXBP1
STXBP1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 Biomarker HPO

Entrez Id: 4644
Gene Symbol: MYO5A
MYO5A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 Biomarker HPO

Entrez Id: 6857
Gene Symbol: SYT1
SYT1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 CausalMutation CLINVAR

Entrez Id: 4574
Gene Symbol: TRNS1
TRNS1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 4549
Gene Symbol: RNR1
RNR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 7468
Gene Symbol: NSD2
NSD2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 5080
Gene Symbol: PAX6
PAX6
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 501
Gene Symbol: ALDH7A1
ALDH7A1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 GeneticVariation CLINVAR

Entrez Id: 1130
Gene Symbol: LYST
LYST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 6515
Gene Symbol: SLC2A3
SLC2A3
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO

Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 GeneticVariation CLINVAR

Entrez Id: 3954
Gene Symbol: LETM1
LETM1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.100 Biomarker HPO