retinal cell programmed cell death

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Results for "retinal cell programmed cell death": 1001 gene sets

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retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ectopic germ cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the ectopic germ cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
programmed necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset.
modulation of programmed cell death in other organism Gene Set From GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
developmental programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation by symbiont of host programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset.
modulation by symbiont of host programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the modulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
modulation of programmed cell death in other organism involved in symbiotic interaction Gene Set From GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset.
induction of programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
host programmed cell death induced by symbiont Gene Set From GO Biological Process Annotations 2015 genes participating in the host programmed cell death induced by symbiont biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation by symbiont of host programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
Programmed cell death protein 2, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Programmed cell death protein 2, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TRIF-mediated programmed cell death Gene Set From Reactome Pathways 2014 proteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways dataset.
Programmed Cell Death Gene Set From Reactome Pathways 2014 proteins participating in the Programmed Cell Death pathway from the Reactome Pathways dataset.
negative regulation of programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
programmed cell death in response to reactive oxygen species Gene Set From GO Biological Process Annotations 2023 genes participating in the programmed cell death in response to reactive oxygen species biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
programmed necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
induction of programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
Diseases of programmed cell death Gene Set From Reactome Pathways 2024 proteins participating in the Diseases of programmed cell death pathway from the Reactome Pathways 2024 dataset.
Programmed Cell Death Gene Set From Reactome Pathways 2024 proteins participating in the Programmed Cell Death pathway from the Reactome Pathways 2024 dataset.
SARS-CoV-1-mediated effects on programmed cell death Gene Set From Reactome Pathways 2024 proteins participating in the SARS-CoV-1-mediated effects on programmed cell death pathway from the Reactome Pathways 2024 dataset.
TLR3-mediated TICAM1-dependent programmed cell death Gene Set From Reactome Pathways 2024 proteins participating in the TLR3-mediated TICAM1-dependent programmed cell death pathway from the Reactome Pathways 2024 dataset.
TRIF-mediated programmed cell death Gene Set From Reactome Pathways 2024 proteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways 2024 dataset.
negative regulation of programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
programmed cell death in response to reactive oxygen species Gene Set From GO Biological Process Annotations 2025 genes participating in the programmed cell death in response to reactive oxygen species biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of programmed necrotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
programmed necrotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
induction of programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of hydrogen peroxide-mediated programmed cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
PROGRAMMED CELL DEATH 1 LIGAND 1 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the PROGRAMMED CELL DEATH 1 LIGAND 1 drug from theDGIdb Drug Targets 2026 dataset.
death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; heart diseases; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; heart diseases; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; myocardial ischemia; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; diabetes mellitus; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Retinal detachment or retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment or retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal detachment with retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment with retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
programmed Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term programmed in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of activated T cell autonomous cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of activated T cell autonomous cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of activated T cell autonomous cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
cytotoxic T cell pyroptotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the cytotoxic T cell pyroptotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of activated T cell autonomous cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
ischemic neuronal cell death Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemic neuronal cell death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
negative regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
activation-induced cell death of t cells Gene Set From GO Biological Process Annotations 2015 genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of hydrogen peroxide-induced cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of activation-induced cell death of t cells Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of activation-induced cell death of t cells Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of activation-induced cell death of t cells Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset.
cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of hydrogen peroxide-induced cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
autophagic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
Cell death regulator Aven Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell death regulator Aven protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal interdigital cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sensitivity to induced cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sensitivity to induced cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal induced cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased activation-induced cell death of t cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal activation-induced cell death of t cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Cell death signalling via NRAGE, NRIF and NADE Gene Set From Reactome Pathways 2014 proteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways dataset.
Stimulation of the cell death response by PAK-2p34 Gene Set From Reactome Pathways 2014 proteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways dataset.
NRIF signals cell death from the nucleus Gene Set From Reactome Pathways 2014 proteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways dataset.
negative regulation of hydrogen peroxide-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2023 genes participating in the activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset.
autophagic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of hydrogen peroxide-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of necrotic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of hydrogen peroxide-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of oxidative stress-induced cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
decreased sensitivity to induced cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased sensitivity to induced cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal interdigital cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cell death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased activation-induced cell death of T cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased activation-induced cell death of T cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Nanoparticle triggered autophagic cell death Gene Set From WikiPathways Pathways 2024 proteins participating in the Nanoparticle triggered autophagic cell death pathway from the WikiPathways Pathways 2024 dataset.
Cell death signalling via NRAGE, NRIF and NADE Gene Set From Reactome Pathways 2024 proteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways 2024 dataset.
FOXO-mediated transcription of cell death genes Gene Set From Reactome Pathways 2024 proteins participating in the FOXO-mediated transcription of cell death genes pathway from the Reactome Pathways 2024 dataset.
NRIF signals cell death from the nucleus Gene Set From Reactome Pathways 2024 proteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways 2024 dataset.
Regulation of necroptotic cell death Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of necroptotic cell death pathway from the Reactome Pathways 2024 dataset.
Stimulation of the cell death response by PAK-2p34 Gene Set From Reactome Pathways 2024 proteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Cell Death Genes Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Cell Death Genes pathway from the Reactome Pathways 2024 dataset.
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain Gene Set From Reactome Pathways 2024 proteins participating in the TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain pathway from the Reactome Pathways 2024 dataset.
activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2025 genes participating in the activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset.
pyroptotic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the pyroptotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
autophagic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of activation-induced cell death of T cells Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of autophagic cell death Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cell cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal cell cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormal retinal rod cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal ganglion cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell inner segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod cell outer segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal progenitor cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal rod cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod bipolar cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal cone cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ganglion cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal ganglion cell Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal ganglion cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal rod cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal rod cell inner segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal cone cell outer segment morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal microvascular endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal microvascular endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal ganglion cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal ganglion cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal stem cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal ganglion cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal ganglion cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Eye-retinal blood vessel endothelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal blood vessel endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal ganglion cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal ganglion cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal pigment epithelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal pigment epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal cone cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal cone cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
Retinal ganglion cell_Ganglion cell layer of retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Ganglion cell layer of retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Superficial retinal vascular plexus (S-tip cell)_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Superficial retinal vascular plexus (S-tip cell)_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal cone cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal cone cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
Retinal cell cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal cell cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal ganglion cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal ganglion cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal stem cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal ganglion cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal ganglion cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal microvascular endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal microvascular endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
Sudden cardiac death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sudden infant death syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
death-inducing signaling complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cd95 death-inducing signaling complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cd95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cd95 death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cd95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
trail death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the trail death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set From CORUM Protein Complexes proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.
Death-inducing signaling complex DISC (type I cells associated), stimulated Gene Set From CORUM Protein Complexes proteins in the Death-inducing signaling complex DISC (type I cells associated), stimulated protein complex from the CORUM Protein Complexes dataset.
Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Set From CORUM Protein Complexes proteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset.
Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Death from the curated CTD Gene-Disease Associations dataset.
Death, Sudden, Cardiac Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Death, Sudden, Cardiac from the curated CTD Gene-Disease Associations dataset.
Fetal Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Death from the curated CTD Gene-Disease Associations dataset.
Death, Sudden Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Death, Sudden from the curated CTD Gene-Disease Associations dataset.
Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome from the curated CTD Gene-Disease Associations dataset.
Sudden Infant Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sudden Infant Death from the curated CTD Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
Death, Sudden, Cardiac Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Death, Sudden, Cardiac in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
sudden infant death syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sudden infant death syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myocardial infarct; cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; death, sudden; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; death, sudden; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sids/sudden infant death syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sids/sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; myocardial infarction; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiac death; cardiac morbidity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiac death; cardiac morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
embryo loss; fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; brain death Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiac arrhythmias and sudden death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiac arrhythmias and sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
staphylococcal infections; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease staphylococcal infections; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; heart diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sudden infant death syndrome (sids) Gene Set From GAD Gene-Disease Associations genes associated with the disease sudden infant death syndrome (sids) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadaver; cardiovascular diseases; death, sudden, cardiac; Gene Set From GAD Gene-Disease Associations genes associated with the disease cadaver; cardiovascular diseases; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of sudden infant death. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy; heart failure; sudden death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart failure; sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden; pulmonary embolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set From GAD Gene-Disease Associations genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; death, sudden, cardiac; Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
long qt syndrome; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; death, sudden; long qt syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death, sudden, cardiac; long qt syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; death, sudden, cardiac; Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism, inborn errors; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sudden infant death syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
death Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term death in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
death Gene Set From GO Biological Process Annotations 2015 genes participating in the death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of hydrogen peroxide-induced neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of hydrogen peroxide-induced neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset.
death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cd95 death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cd95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
death receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
death effector domain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
death domain binding Gene Set From GO Molecular Function Annotations 2015 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
death receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Aging (time to death) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sudden cardiac death Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sudden cardiac death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
time of death Gene Set From GWASdb SNP-Phenotype Associations genes associated with the time of death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sudden death Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sudden death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sudden cardiac death Gene Set From HPO Gene-Disease Associations genes associated with the sudden cardiac death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal death Gene Set From HPO Gene-Disease Associations genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in childhood Gene Set From HPO Gene-Disease Associations genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in infancy Gene Set From HPO Gene-Disease Associations genes associated with the death in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
time of death Gene Set From HPO Gene-Disease Associations genes associated with the time of death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sudden death Gene Set From HPO Gene-Disease Associations genes associated with the sudden death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in early adulthood Gene Set From HPO Gene-Disease Associations genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Brain Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Brain Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Death, Sudden, Cardiac Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Death, Sudden, Cardiac phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Death, Sudden Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Death, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sudden Infant Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sudden Infant Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Death-like domain of Spt6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Death-like domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Death domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Death domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Domain of unknown function DUF2428, death-receptor-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF2428, death-receptor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Death-associated protein kinase 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-associated protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BH3-interacting domain death agonist Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the BH3-interacting domain death agonist protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Death effector domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Death effector domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Caffeine-induced death protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Caffeine-induced death protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
premature death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pregnancy-related premature death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{sudden infant death syndrome, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {sudden infant death syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
sudden infant death with dysgenesis of the testes syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation, developmental delay, coarse facies, and early death Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.
death Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term death in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Death Receptor Signalling Gene Set From Reactome Pathways 2014 proteins participating in the Death Receptor Signalling pathway from the Reactome Pathways dataset.
NADE modulates death signalling Gene Set From Reactome Pathways 2014 proteins participating in the NADE modulates death signalling pathway from the Reactome Pathways dataset.
NRAGE signals death through JNK Gene Set From Reactome Pathways 2014 proteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways dataset.
Sudden Unexplained Death In Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Infant Death Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Infant Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexplained Death In Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexpected Nocturnal Death Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexpected Nocturnal Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexplained Infant Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Infant Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Infant Death With Dysgenesis Of The Testes Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Infant Death With Dysgenesis Of The Testes Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Death In Infancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death In Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Cardiac Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death In Early Adulthood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Early Adulthood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Risk Of Sudden Cardiac Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Risk Of Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cardiac Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Determination Of Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Determination Of Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death Anxiety Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death Anxiety in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Embryo Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Brain Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Near Sudden Infant Death Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Near Sudden Infant Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unexplained Sudden Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unexplained Sudden Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Perinatal Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perinatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aborted Sudden Cardiac Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aborted Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Arrhythmic Death Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Arrhythmic Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infant Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infant Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of hydrogen peroxide-induced neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of hydrogen peroxide-induced neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of oxidative stress-induced neuron death Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
CD95 death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the CD95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
death receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
death receptor agonist activity Gene Set From GO Molecular Function Annotations 2023 genes performing the death receptor agonist activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
death domain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
death receptor binding Gene Set From GO Molecular Function Annotations 2023 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
death effector domain binding Gene Set From GO Molecular Function Annotations 2023 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
premature death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pregnancy-related premature death Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sudden unexpected death in epilepsy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sudden unexpected death in epilepsy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Sudden infant death syndrome SIDS susceptibility pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Sudden infant death syndrome SIDS susceptibility pathways pathway from the WikiPathways Pathways 2024 dataset.
Caspase activation via Death Receptors in the presence of ligand Gene Set From Reactome Pathways 2024 proteins participating in the Caspase activation via Death Receptors in the presence of ligand pathway from the Reactome Pathways 2024 dataset.
Death Receptor Signaling Gene Set From Reactome Pathways 2024 proteins participating in the Death Receptor Signaling pathway from the Reactome Pathways 2024 dataset.
NADE modulates death signalling Gene Set From Reactome Pathways 2024 proteins participating in the NADE modulates death signalling pathway from the Reactome Pathways 2024 dataset.
NRAGE signals death through JNK Gene Set From Reactome Pathways 2024 proteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways 2024 dataset.
TP53 Regulates Transcription of Death Receptors and Ligands Gene Set From Reactome Pathways 2024 proteins participating in the TP53 Regulates Transcription of Death Receptors and Ligands pathway from the Reactome Pathways 2024 dataset.
extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset.
death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of death-inducing signaling complex assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
CD95 death-inducing signaling complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the CD95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
death receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
death receptor agonist activity Gene Set From GO Molecular Function Annotations 2025 genes performing the death receptor agonist activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
death receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
death domain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
death effector domain binding Gene Set From GO Molecular Function Annotations 2025 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Sudden infant death syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sudden infant death syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
death-inducing signaling complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
CD95 death-inducing signaling complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the CD95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
CD95 death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the CD95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
TRAIL death-inducing signaling complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the TRAIL death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Sudden unexplained death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SUDDEN INFANT DEATH SYNDR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SUDDEN INFANT DEATH SYNDR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sudden cardiac death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Death in early adulthood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in early adulthood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Family history of sudden cardiac death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Family history of sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurodegenerative illness progressing to crippling dystonia and death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodegenerative illness progressing to crippling dystonia and death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sudden infant death-dysgenesis of the testes syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden infant death-dysgenesis of the testes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sudden unexplained death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiovascular death or myocardial infarction in response to clopidogrel treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular death or myocardial infarction in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aging (time to death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (mother's age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (father's age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (father's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (combined parental age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (combined parental age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (mother's age at death or mother's attained age) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death or mother's attained age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhegmatogenous retinal detachment, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal degeneration, autosomal recessive, clumped pigment type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
retinal dimer Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical retinal dimer from the curated CTD Gene-Chemical Interactions dataset.
9-cis-retinal Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.
13-cis-retinal Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 13-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.
Retinal Cone Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
Retinal Detachment Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Detachment from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, retinal, 1, North Carolina type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.
Retinal Artery Occlusion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Artery Occlusion from the curated CTD Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy from the curated CTD Gene-Disease Associations dataset.
Macular Dystrophy, Retinal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.
Retinal Dystrophies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Dystrophies from the curated CTD Gene-Disease Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.
Retinal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Diseases from the curated CTD Gene-Disease Associations dataset.
MACULAR DYSTROPHY, RETINAL, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Retinal Vein Occlusion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Vein Occlusion from the curated CTD Gene-Disease Associations dataset.
Doyne honeycomb retinal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.
RETINAL DYSPLASIA, PRIMARY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.
Retinal cone dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Retinal Telangiectasis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Telangiectasis from the curated CTD Gene-Disease Associations dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.
Retinal Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Retinal Vein Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Retinal Vein in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
retinal cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal vascular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal microaneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal microaneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vascular occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vascular occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
abnormal retinal correspondence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal perforation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acute retinal necrosis syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute retinal necrosis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal vascular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
branch retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease branch retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal hemangioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal hemangioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal detachment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal detachment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetes complications; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
branch retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease branch retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal function Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing loss/deafness; retinal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; retinal vascular occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal detachment; vitreoretinopathy, proliferative Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal detachment; vitreoretinopathy, proliferative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vascular occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vascular occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal detachment Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal detachment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
night blindness; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease night blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; retinal vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
color vision defects; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet's disease; retinal vasculitis; uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet's disease; retinal vasculitis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal artery occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal neoplasms; retinoblastoma Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal neoplasms; retinoblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vascular occlusive disease Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vascular occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neovascularization, pathologic; retinal vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease neovascularization, pathologic; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; inflammation; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; inflammation; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal dystrophies; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal dystrophies; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term retinal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
retinal bipolar neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal isomerase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
all-trans-retinal Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the all-trans-retinal ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Retinal vascular caliber Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Rhegmatogenous retinal detachment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
retinal degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal detachment Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal detachment in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal vascular disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal vascular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of retinal arteries Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
retinal coloboma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the retinal coloboma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
rhegmatogenous retinal detachment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
retinal detachment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the retinal vasculature Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
4-OH-Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the 4-OH-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
9-cis-Retinal Gene Set From HMDB Metabolites of Enzymes interacting proteins for the 9-cis-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.
retinal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal striation Gene Set From HPO Gene-Disease Associations genes associated with the retinal striation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacunar retinal depigmentation Gene Set From HPO Gene-Disease Associations genes associated with the lacunar retinal depigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal retinal infarction Gene Set From HPO Gene-Disease Associations genes associated with the focal retinal infarction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
exudative retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the exudative retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tractional retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the tractional retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macroreticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macroreticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rarefaction of retinal pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the rarefaction of retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal retinal folds Gene Set From HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large hyperpigmented retinal spots Gene Set From HPO Gene-Disease Associations genes associated with the large hyperpigmented retinal spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal telangiectasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal telangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal pigmentation abnormalities Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal pigmentation abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the absent retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
depigmented lesions of the retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the depigmented lesions of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
achromatic retinal patches Gene Set From HPO Gene-Disease Associations genes associated with the achromatic retinal patches phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal calcification Gene Set From HPO Gene-Disease Associations genes associated with the retinal calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular malformation Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the retinal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal flecks Gene Set From HPO Gene-Disease Associations genes associated with the retinal flecks phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar constriction Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar constriction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal avascularization Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal avascularization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal pigment epithelial atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal nonattachment Gene Set From HPO Gene-Disease Associations genes associated with the retinal nonattachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased retinal pigmentation with dispersion Gene Set From HPO Gene-Disease Associations genes associated with the decreased retinal pigmentation with dispersion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal malformation Gene Set From HPO Gene-Disease Associations genes associated with the retinal malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
falciform retinal fold Gene Set From HPO Gene-Disease Associations genes associated with the falciform retinal fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital hypertrophy of retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the congenital hypertrophy of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the retinal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of retinal pigment epithelium Gene Set From HPO Gene-Disease Associations genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal deposits Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the retinal vasculature Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the retinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular retinal pigment epithelial mottling Gene Set From HPO Gene-Disease Associations genes associated with the macular retinal pigment epithelial mottling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal retinal pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal arteriolar occlusion Gene Set From HPO Gene-Disease Associations genes associated with the retinal arteriolar occlusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the reticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of retinal arteries Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of retinal arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rhegmatogenous retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the rhegmatogenous retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
honeycomb retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the honeycomb retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypermyelinated retinal fibers Gene Set From HPO Gene-Disease Associations genes associated with the hypermyelinated retinal fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal coloboma Gene Set From HPO Gene-Disease Associations genes associated with the retinal coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal exudate Gene Set From HPO Gene-Disease Associations genes associated with the retinal exudate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hamartoma Gene Set From HPO Gene-Disease Associations genes associated with the retinal hamartoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystic retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal vascular proliferation Gene Set From HPO Gene-Disease Associations genes associated with the retinal vascular proliferation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
attenuation of retinal blood vessels Gene Set From HPO Gene-Disease Associations genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral traction retinal detachment Gene Set From HPO Gene-Disease Associations genes associated with the peripheral traction retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal hemangioblastoma Gene Set From HPO Gene-Disease Associations genes associated with the retinal hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Retinal Detachment Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Detachment phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Artery Occlusion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Artery Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Dystrophies Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Dystrophies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Vein Occlusion Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Vein Occlusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Drusen Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Drusen phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Vasculitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Vasculitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Neovascularization Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Neovascularization phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Perforations Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Perforations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal pigment epithelium GPCR Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal pigment epithelium GPCR protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal-specific ATP-binding cassette transporter Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal protein C2orf71 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal cGMP phosphodiesterase, gamma subunit Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal cGMP phosphodiesterase, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Visual pigments (opsins) retinal binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal degeneration protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal retinal photoreceptor layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner nuclear layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal melanocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal inner plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal neuronal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal neuronal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer nuclear layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal outer nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal rod cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thick retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thick retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal layers Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal layers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal photoreceptor morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal blood vessel morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal deposits Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal induced retinal neovascularization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal ganglion layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ischemia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ischemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal outer nuclear layer degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal detachment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal detachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal gliosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal gliosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal inner nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal vasculature morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal vasculature morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer plexiform layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retinal cone cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retinal cone cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal outer nuclear layer thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal outer nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal spots Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal spots phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal blood vessel pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal inner plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced retinal damage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal nerve fiber layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal nerve fiber layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal photoreceptor degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal photoreceptor degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal outer plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal outer nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal pigment epithelium morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin retinal outer plexiform layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner plexiform layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal inner nuclear layer thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal inner nuclear layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal neovascularization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized retinal ganglion layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal melanin granule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{retinal disease in usher syndrome type iia, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
bothnia retinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, late-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal nonattachment, nonsyndromic congenital Gene Set From OMIM Gene-Disease Associations genes associated with the retinal nonattachment, nonsyndromic congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, autosomal recessive, clumped pigment type Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal cone dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3b Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
vasculopathy, retinal, with cerebral leukodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
Biosynthesis of A2E, implicated in retinal degradation Gene Set From Reactome Pathways 2014 proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways dataset.
retinal rod Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal rod from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal pigment epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal cone Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retinal cone from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retinal pigment epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal pigment epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal cone Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retinal rod Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retinal rod in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Neural retinal development(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Neural retinal development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eye-retinal bipolar neuron Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal bipolar neuron relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Retinal Astrocytic Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Astrocytic Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelial Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelial Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelium Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Toxicity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Toxicity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Venous Retinal Branch Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Venous Retinal Branch Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Necrosis Syndrome, Acute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Necrosis Syndrome, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Retinal Degeneration (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Serous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Serous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Dysplasia And Retinal Aplasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Angiomatous Proliferation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Angiomatous Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Drusen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Retinal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Retinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypertrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypertrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vasculitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vasculitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment, Nonsyndromic Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Hyperpigmented Retinal Spots Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Large Hyperpigmented Retinal Spots in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Lattice Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Lattice Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Amaurosis Of Retinal Origin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Amaurosis Of Retinal Origin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Juxtafoveal Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Juxtafoveal Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patterned Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patterned Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmentary Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmentary Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion - Juvenile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion - Juvenile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Retinal Fold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Retinal Fold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Microaneurysm With Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Microaneurysm With Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Gliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vascular Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vascular Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Arteriovenous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Microaneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Microaneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Thickening Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thickening in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bothnia Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Retinal Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Retinal Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonperfusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonperfusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Retinal Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Retinal Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Retinal Pigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Retinal Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Attenuation Of Retinal Blood Vessels Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Attenuation Of Retinal Blood Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Flecking Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Flecking in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Mottling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Mottling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Thinning Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Thinning in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peau D'Orange Retinal Changes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peau D'Orange Retinal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Damage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Damage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Depigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Depigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Crystals Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Crystals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choroidal Retinal Neovascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choroidal Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Fold (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Fold (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Retinal Vessel Vascular Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Retinal Vessel Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteriolar Occlusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteriolar Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Neovascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigmentary Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arteries, Tortuosity Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arteries, Tortuosity Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypoautofluorescent Retinal Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypoautofluorescent Retinal Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Retinal Avascularization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Retinal Avascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Exudates Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Exudates in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Achromatic Retinal Patches Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Achromatic Retinal Patches in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arterial Macroaneurysms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arterial Macroaneurysms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Proliferation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Dots Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Dots in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Vascular Malformation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Cystoid Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Cystoid Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypermyelinated Retinal Nerve Fibers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermyelinated Retinal Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Tractional Retinal Detachment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Tractional Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
establishment of blood-retinal barrier Gene Set From GO Biological Process Annotations 2023 genes participating in the establishment of blood-retinal barrier biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2023 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2023 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2023 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
all-trans retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the all-trans retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
11-cis-retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 11-cis-retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
Retinal Gene Set From MW Enzyme Metabolite Associations interacting proteins for Retinal metabolite from the MW Gene Metabolite Associations dataset.
9-cis-Retinal Gene Set From MW Enzyme Metabolite Associations interacting proteins for 9-cis-Retinal metabolite from the MW Gene Metabolite Associations dataset.
Human - Fetal Development - L1 - Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Retinal ganglion cell_Cerebral organoid_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Cerebral organoid_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Embryonic stem cell_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Embryonic stem cell_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal progenitor cell_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal progenitor cell_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal astrocyte_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal astrocyte_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Neurogenic retinal progenitor cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neurogenic retinal progenitor cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Multipotent retinal progenitor cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Multipotent retinal progenitor cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelium_Retina_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelium_Retina_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelial cell_Choroid_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelial cell_Choroid_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Eye_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal pigment epithelial cell_Eye_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal pigment epithelial cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal Müller glia cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal Müller glia cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinal ganglion cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinal ganglion cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
GPR143 in melanocytes and retinal pigment epithelium cells Gene Set From WikiPathways Pathways 2024 proteins participating in the GPR143 in melanocytes and retinal pigment epithelium cells pathway from the WikiPathways Pathways 2024 dataset.
EPAC1 and PKA reduction of retinal inflammation Gene Set From WikiPathways Pathways 2024 proteins participating in the EPAC1 and PKA reduction of retinal inflammation pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis of A2E, implicated in retinal degradation Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways 2024 dataset.
establishment of blood-retinal barrier Gene Set From GO Biological Process Annotations 2025 genes participating in the establishment of blood-retinal barrier biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2025 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
all-trans retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the all-trans retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
11-cis-retinal 3,4-desaturase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 11-cis-retinal 3,4-desaturase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Retinal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary retinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal vascular disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal detachment Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal detachment in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal vascular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal lattice degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal lattice degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal detachment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal detachment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal perforation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute retinal necrosis syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute retinal necrosis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal ischemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular retinal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular retinal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vascular occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vascular occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Doyne honeycomb retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
late-onset retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease late-onset retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal telangiectasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Branch retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Branch retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal dystrophy with leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal dystrophy with leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal vasculopathy with cerebral leukodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal vasculopathy with cerebral leukodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal macular dystrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal macular dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bothnia retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bothnia retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystrophies primarily involving the retinal pigment epithelium Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystrophies primarily involving the retinal pigment epithelium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal arterial tortuosity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal arterial tortuosity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Abnormal retinal correspondence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic disc anomalies with retinal and/or macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic disc anomalies with retinal and/or macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal microaneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal microaneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal hemangioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal hemangioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal cone dystrophy 3B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal cone dystrophy 3B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient retinal arterial occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient retinal arterial occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cobblestone retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cobblestone retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal pigment epithelium Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal pigment epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cone Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal cone from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal rod Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retinal rod from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal rod Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal rod in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal pigment epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal pigment epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal cone Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retinal cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal dysplasia and retinal aplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal dysplasia and retinal aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-onset retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-onset retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal pigment epithelial atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early onset and severe retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset and severe retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal vasculopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal vasculopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-childhood-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic inherited retinal disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic inherited retinal disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal akinesia-cerebral and retinal hemorrhage syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal akinesia-cerebral and retinal hemorrhage syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmentary retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmentary retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Doyne honeycomb retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Doyne honeycomb retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bothnia retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bothnia retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Patterned dystrophy of the retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Patterned dystrophy of the retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant rhegmatogenous retinal detachment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant rhegmatogenous retinal detachment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal cone dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal cone dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormality of retinal pigmentation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of retinal pigmentation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Harmonizome 3.0

retinal cell programmed cell death Gene Set

regulation of retinal cell programmed cell death Gene Set

negative regulation of retinal cell programmed cell death Gene Set

coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set

ectopic germ cell programmed cell death Gene Set

regulation of programmed cell death Gene Set

positive regulation of programmed cell death Gene Set

negative regulation of programmed cell death Gene Set

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set

programmed necrotic cell death Gene Set

positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

modulation of programmed cell death in other organism Gene Set

positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set

developmental programmed cell death Gene Set

regulation of hydrogen peroxide-mediated programmed cell death Gene Set

positive regulation by symbiont of host programmed cell death Gene Set

negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

modulation by symbiont of host programmed cell death Gene Set

modulation of programmed cell death in other organism involved in symbiotic interaction Gene Set

induction of programmed cell death Gene Set

host programmed cell death induced by symbiont Gene Set

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

negative regulation by symbiont of host programmed cell death Gene Set

programmed cell death Gene Set

Programmed cell death protein 2, C-terminal Gene Set

TRIF-mediated programmed cell death Gene Set

Programmed Cell Death Gene Set

negative regulation of programmed cell death Gene Set

negative regulation of programmed necrotic cell death Gene Set

positive regulation of programmed cell death Gene Set

regulation of programmed cell death Gene Set

negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

programmed cell death in response to reactive oxygen species Gene Set

regulation of programmed necrotic cell death Gene Set

programmed necrotic cell death Gene Set

induction of programmed cell death Gene Set

positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set

hydrogen peroxide-mediated programmed cell death Gene Set

positive regulation of programmed necrotic cell death Gene Set

regulation of hydrogen peroxide-mediated programmed cell death Gene Set

Diseases of programmed cell death Gene Set

Programmed Cell Death Gene Set

SARS-CoV-1-mediated effects on programmed cell death Gene Set

TLR3-mediated TICAM1-dependent programmed cell death Gene Set

TRIF-mediated programmed cell death Gene Set

negative regulation of programmed cell death Gene Set

negative regulation of programmed necrotic cell death Gene Set

positive regulation of programmed cell death Gene Set

regulation of programmed cell death Gene Set

negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

programmed cell death in response to reactive oxygen species Gene Set

regulation of programmed necrotic cell death Gene Set

positive regulation of programmed necrotic cell death Gene Set

programmed necrotic cell death Gene Set

induction of programmed cell death Gene Set

hydrogen peroxide-mediated programmed cell death Gene Set

regulation of hydrogen peroxide-mediated programmed cell death Gene Set

PROGRAMMED CELL DEATH 1 LIGAND 1 Gene Set

death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene Set

death, sudden, cardiac; heart diseases; sudden cardiac death Gene Set

death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set

death, sudden; sudden infant death Gene Set

arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene Set

fetal death; sudden infant death Gene Set

chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set

death; sudden infant death Gene Set

death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene Set

arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene Set

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

death, sudden, cardiac; sudden cardiac death Gene Set

death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set