Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7124
Gene Symbol: TNF
TNF
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker LHGDN Inflammation at birth is associated with subnormal development in very preterm infants. 18391842

2008

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR Homozygosity for MECP2 gene in a girl with classical Rett syndrome. 17881312

2008

Entrez Id: 3569
Gene Symbol: IL6
IL6
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker LHGDN Inflammation at birth is associated with subnormal development in very preterm infants. 18391842

2008

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome. 17089071

2007

Entrez Id: 7124
Gene Symbol: TNF
TNF
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation BEFREE Carriage of polymorphisms in the tumor necrosis factor-alpha and mannose-binding lectin genes are associated with an increased risk of cerebral palsy. 16522396

2006

Entrez Id: 7124
Gene Symbol: TNF
TNF
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker BEFREE Factor 5, Factor 2, methylene tetrahydrofolate reductase, tumor necrosis factor-alpha, and other SNPs tested were not significantly associated with CP risk. 15718364

2005

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR Prenatal diagnosis in Rett syndrome. 12065946

2003

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR Chronic osteomyelitis in patients with sickle cell disease. 10944834

2000

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 CausalMutation CLINVAR

Entrez Id: 1776
Gene Symbol: DNASE1L3
DNASE1L3
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 5624
Gene Symbol: PROC
PROC
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 51102
Gene Symbol: MECR
MECR
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 CausalMutation CLINVAR

Entrez Id: 3673
Gene Symbol: ITGA2
ITGA2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 5373
Gene Symbol: PMM2
PMM2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 CausalMutation CLINVAR

Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 767
Gene Symbol: CA8
CA8
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 54941
Gene Symbol: RNF125
RNF125
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 2812
Gene Symbol: GP1BB
GP1BB
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR

Entrez Id: 10382
Gene Symbol: TUBB4A
TUBB4A
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 GeneticVariation CLINVAR

Entrez Id: 23389
Gene Symbol: MED13L
MED13L
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 CausalMutation CLINVAR

Entrez Id: 6578
Gene Symbol: SLCO2A1
SLCO2A1
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO

Entrez Id: 124997
Gene Symbol: WDR81
WDR81
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.100 Biomarker HPO