Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C4014492
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 		0.700 CausalMutation CLINVAR

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.110 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0423113
Disease: Telecanthus
Telecanthus 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1836543
Disease: Thick vermilion border
Thick vermilion border 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1848529
Disease: Hypoplasia of the pons
Hypoplasia of the pons 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1857970
Disease: Hypobetalipoproteinemia, Familial, 2
Hypobetalipoproteinemia, Familial, 2 		0.100 CausalMutation CLINVAR

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1861324
Disease: Short philtrum
Short philtrum 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C3810365
Disease: Central visual impairment
Central visual impairment 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR The Rac activator DOCK7 regulates neuronal polarity through local phosphorylation of stathmin/Op18. 16982419

2006
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 GeneticVariation CLINVAR The Rac activator DOCK7 regulates neuronal polarity through local phosphorylation of stathmin/Op18. 16982419

2006
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.100 GeneticVariation GWASDB Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. 18179892

2008
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation GWASCAT Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 18193043

2008
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation GWASDB Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 18193043

2008
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009