Name

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.

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 blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

abnormal kidney venous blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney venous blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel elastic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel elastic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney arterial blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney arterial blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal umbilical cord blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal umbilical cord blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urinary bladder blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urinary bladder blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood vessel endothelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel development biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel development biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

labyrinthine layer blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the labyrinthine layer blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration involved in intussusceptive angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration involved in intussusceptive angiogenesis biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel lumenization Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel lumenization biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of testicular blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of testicular blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

placenta blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the placenta blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate specification biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel maturation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in blood vessel relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

blood vessel endothelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood vessel endothelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood vessel Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood vessel from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood vessel endothelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel endothelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

blood vessel wall Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

blood vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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.

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.

apoptotic process involved in patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic process involved in patterning of blood vessels biological process from the curated GO Biological Process Annotations dataset.

patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the patterning of blood vessels biological process from the curated GO Biological Process Annotations 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.

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 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.

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.

abnormal coronary vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal coronary vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal afferent lymphatic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal afferent lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel smooth muscle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel smooth muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intersomitic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intersomitic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart and great vessel attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart and great vessel attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel endothelial cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

blood pressure, oxidative stress levels in blood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, oxidative stress levels in blood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood and blood forming organ disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood and blood-forming tissues Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal branching pattern of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pattern of respiration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acquired abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sympathetic neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mammary gland pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dorsoventral coat patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dorsoventral coat patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal non-rapid eye movement sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urination pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urination pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain wave pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rostral-caudal axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal rostral-caudal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal central pattern generator function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal breathing pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal breathing pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ihc efferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ihc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sensory neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sensory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dorsal-ventral axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dorsal-ventral axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal paradoxical sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rostral-caudal patterning of the somites Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal rostral-caudal patterning of the somites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ihc afferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ihc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal left-right axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal left-right axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal innervation pattern to muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal innervation pattern to muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal developmental patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal developmental patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal patterning of the organ of corti Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal patterning of the organ of corti phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal proximal-distal axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal olfactory neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal phrenic nerve innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal phrenic nerve innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ohc efferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ohc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enamel rod pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enamel rod pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motor neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal phrenic nerve innervation pattern to diaphragm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal phrenic nerve innervation pattern to diaphragm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ohc afferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ohc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Brain small vessel disease with hemorrhage Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain Small Vessel Disease with Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Vessel Anomalies from the curated CTD Gene-Disease Associations dataset.

vessel stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vessel stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral small-vessel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary vessel anomalies; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary vessel anomalies; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke, lacunar; small-vessel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vessel Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term vessel in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

lymph vessel development Gene Set

From GO Biological Process Annotations

genes participating in the lymph vessel development biological process from the curated GO Biological Process Annotations dataset.

lymph vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the lymph vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

large vessel vasculitis Gene Set

From HPO Gene-Disease Associations

genes associated with the large vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small vessel vasculitis Gene Set

From HPO Gene-Disease Associations

genes associated with the small vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral pulmonary vessel aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral pulmonary vessel aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Coronary Vessel Anomalies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

enlarged lymphatic vessel Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged lymphatic vessel phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lymphatic vessel endothelial cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lymphatic vessel endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lymphatic vessel hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lymphatic vessel hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

plant vessel Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue plant vessel from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

plant vessel Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue plant vessel in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

lymph vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue lymph vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

seed vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue seed vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

plant vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue plant vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

male-pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male-pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prostate volume/histology endocrine patterns Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prostate volume/histology endocrine patterns in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovaries and premature male pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovaries and premature male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pattern Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term pattern in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patternsof Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patternsof in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patterns Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patterns in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patternare Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patternare in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patterning Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patterning in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patterned Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patterned in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

patternrecognition Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term patternrecognition in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

embryonic heart tube anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation involved in nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations dataset.

dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

anterior compartment pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations dataset.

cytoplasmic pattern recognition receptor signaling pathway in response to virus Gene Set

From GO Biological Process Annotations

genes participating in the cytoplasmic pattern recognition receptor signaling pathway in response to virus biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation involved in metanephric nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

rostrocaudal neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the rostrocaudal neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

lung pattern specification process Gene Set

From GO Biological Process Annotations

genes participating in the lung pattern specification process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

neural plate pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate pattern specification biological process from the curated GO Biological Process Annotations dataset.

cell fate commitment involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate commitment involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

compartment pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the compartment pattern specification biological process from the curated GO Biological Process Annotations dataset.

cell fate specification involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate specification involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

embryonic pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic pattern specification biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in metanephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in metanephros development biological process from the curated GO Biological Process Annotations dataset.

forebrain dorsal/ventral pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the forebrain dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations dataset.

radial pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the radial pattern formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

dorsal/ventral pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations dataset.

bmp signaling pathway involved in spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the bmp signaling pathway involved in spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in mesonephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in mesonephros development biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

cell surface pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the cell surface pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

pattern specification process Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification process biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in ureteric bud development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

forebrain anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in pronephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in pronephros development biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

cell fate determination involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate determination involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

signaling pattern recognition receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the signaling pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

pattern binding Gene Set

From GO Molecular Function Annotations

genes performing the pattern binding molecular function from the curated GO Molecular Function Annotations dataset.

pattern recognition receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Male-pattern baldness Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

termporal pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the termporal pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

reduced amplitude of pattern visual evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

termporal pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the termporal pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Pattern Recognition, Physiological Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pattern Recognition, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Pattern Recognition, Visual Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pattern Recognition, Visual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

distorted hair follicle pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

macular dystrophy, patterned, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

abnormal concentration of calcium in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal levels of creatine kinase in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal umbilical cord blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal blood gas level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal systemic arterial blood pressure regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal systemic arterial blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-brain barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-brain barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood ph regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood ph regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-inner ear barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood flow velocity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood flow velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood coagulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood coagulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood circulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood circulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood cell morphology/development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood homeostasis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta fetal blood space morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-cerebrospinal fluid barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-cerebrospinal fluid barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell deformability Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell deformability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal visceral yolk sac blood island morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal visceral yolk sac blood island morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood pressure regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circadian regulation of systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circadian regulation of systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations 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.

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.

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 Assocation 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 Assocation Evidence Scores

genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal cell cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease retinal cell cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

retinal disease Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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.

retinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

retinal hemangioblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Assocation 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 Assocation 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.

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.

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.

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

retinal bipolar neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

retinal pigment epithelium development Gene Set

From GO Biological Process Annotations

genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations dataset.

retinal metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations dataset.

retinal cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal cone cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations dataset.

retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations dataset.

retinal dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

retinal isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

all-trans retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

11-cis retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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 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.

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 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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

{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

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 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 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 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 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.

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.

Neural retinal development(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Neural retinal development(Mus musculus) pathway from the Wikipathways Pathways dataset.

Blood group, john milton hagen system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, john milton hagen system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WALDNER TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cromer blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Radin blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radin blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, junior system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, junior system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, gerbich system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, gerbich system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--OK Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--OK phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antigen in Scianna blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antigen in Scianna blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Langereis blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--FROESE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--FROESE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--LUTHERAN INHIBITOR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--LUTHERAN INHIBITOR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, dombrock system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, dombrock system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WRIGHT ANTIGEN Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WRIGHT ANTIGEN phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

blood microparticle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the blood microparticle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

blood microparticle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the blood microparticle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dragon's blood Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical dragon's blood from the curated CTD Gene-Chemical Interactions dataset.

Blood Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Blood Glucose from the curated CTD Gene-Chemical Interactions dataset.

Blood Loss, Surgical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Loss, Surgical from the curated CTD Gene-Disease Associations dataset.

Blood Coagulation Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Coagulation Disorders from the curated CTD Gene-Disease Associations dataset.

Blood Platelet Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Platelet Disorders from the curated CTD Gene-Disease Associations dataset.

PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL from the curated CTD Gene-Disease Associations dataset.

Blood Coagulation Disorders, Inherited Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Coagulation Disorders, Inherited from the curated CTD Gene-Disease Associations dataset.

Blood Viscosity Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Viscosity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Cells Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Cells in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Proteins Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Glucose Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Glucose in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Urea Nitrogen Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Urea Nitrogen in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Coagulation Factors Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Coagulation Factors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Pressure Determination Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Pressure Determination in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Sedimentation Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Sedimentation in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Flow Velocity Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Flow Velocity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Vessels Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Vessels in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Pressure Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Pressure in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Coagulation Factor Inhibitors Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Coagulation Factor Inhibitors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

blood platelet disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood platelet disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood protein disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood protein disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

inherited blood coagulation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease inherited blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease blood coagulation disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

blood group incompatibility Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood group incompatibility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

inherited blood coagulation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease inherited blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of blood Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of blood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood platelet disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood platelet disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood protein disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood protein disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood platelet disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood platelet disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl/blood* Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl/blood* in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood group incompatibility; rh isoimmunization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood group incompatibility; rh isoimmunization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate; orthostatic intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate; orthostatic intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

baroreflex and blood pressure regulation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease baroreflex and blood pressure regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; left ventricular function; blood pressure; left ventricular structure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; blood pressure, arterial; antioxidant activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; blood pressure, arterial; antioxidant activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; heart rate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; carotid atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; carotid atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; blood pressure, arterial; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood urea nitrogen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood urea nitrogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood catalase levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood catalase levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; arterial wall changes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; arterial wall changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; inflammation; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; inflammation; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead blood levels; zinc Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lead blood levels; zinc in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; triglycerides; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood loss, surgical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood loss, surgical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood viscosity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood viscosity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; osteonecrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; osteonecrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; left ventricular mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood sedimentation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood sedimentation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

systolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow velocity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow velocity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood lipids and maximal oxygen uptake Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood lipids and maximal oxygen uptake in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; blood pressure; atherosclerosis, carotid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; blood pressure; atherosclerosis, carotid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure determination Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure determination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoproliferative disorders; blood transfusion complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoproliferative disorders; blood transfusion complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary blood flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary blood flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macroangiopathy and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macroangiopathy and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood transfusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood transfusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ace concentration and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ace concentration and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progression of carotid atherosclerosis blood pressure and serum lipids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease progression of carotid atherosclerosis blood pressure and serum lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation factor inhibitors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation factor inhibitors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; blood pressure, arterial; stroke; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; blood pressure, arterial; stroke; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adiposity and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adiposity and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood platelet disorders; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood platelet disorders; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; sodium hemostatis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; sodium hemostatis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; renin activity; aldosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; renin activity; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial; sleep apnea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood group incompatibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood group incompatibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; blood pressure; endothelin-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; blood pressure; endothelin-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cord blood igf-ii levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cord blood igf-ii levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood flow; left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood flow; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

i/d ace gene polymorphism and abo blood group system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease i/d ace gene polymorphism and abo blood group system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated fasting blood glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated fasting blood glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephropathy, diabetic; blood pressure, arterial; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy, diabetic; blood pressure, arterial; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; lipids; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; lipids; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol, hdl; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol, hdl; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood proteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid in plasma and red blood cell folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial diabetes, type 2 glucose insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial diabetes, type 2 glucose insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased blood pressure and plasma triglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood transfusion complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood transfusion complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

higher blood pressure after hospitalization in normotensi Gene Set

From GAD Gene-Disease Associations

genes associated with the disease higher blood pressure after hospitalization in normotensi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; nitric oxide production; salt sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sleep disorders; body mass; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood dioxin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood dioxin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood lead concentration in children. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood lead concentration in children. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure phenotypes. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure phenotypes. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; aldosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood pressure, arterial; nephropathy in other diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood pressure, arterial; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diastolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diastolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood cells Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood cells in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sex steroid hormone blood levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sex steroid hormone blood levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; diabetes, type 2; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; diabetes, type 2; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood vessels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood tacrolimus concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood tacrolimus concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; insulin; obesity; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; insulin; obesity; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated blood pressure and personality disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated blood pressure and personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

c-reactive protein blood levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease c-reactive protein blood levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; triglycerides; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; triglycerides; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol abuse; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol abuse; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass index, blood pressure and cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass index, blood pressure and cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term blood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Bacterial Infection_Peripheral blood mononuclear cell_GSE3026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Bacterial Infection_Peripheral blood mononuclear cell_GSE3026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

HIV - Human immunodeficiency virus infection_Peripheral blood mononuclear cell_GSE2171 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during HIV - Human immunodeficiency virus infection_Peripheral blood mononuclear cell_GSE2171 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Ulcerative Colitis_Peripheral blood mononuclear cell_GSE3365 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Ulcerative Colitis_Peripheral blood mononuclear cell_GSE3365 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

PFKL_OE_GDS3353_76_human_B cells in blood Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PFKL_OE_GDS3353_76_human_B cells in blood gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of blood coagulation, intrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of blood microparticle formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood microparticle formation biological process from the curated GO Biological Process Annotations dataset.

renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

establishment of glial blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of glial blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

establishment of blood-nerve barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of blood-nerve barrier biological process from the curated GO Biological Process Annotations dataset.

renal system process involved in regulation of blood volume Gene Set

From GO Biological Process Annotations

genes participating in the renal system process involved in regulation of blood volume biological process from the curated GO Biological Process Annotations dataset.

angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

maintenance of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, extrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, extrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

negative regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure mediated by a chemical signal Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure mediated by a chemical signal biological process from the curated GO Biological Process Annotations dataset.

regulation of blood volume by renal aldosterone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood volume by renal aldosterone biological process from the curated GO Biological Process Annotations dataset.

renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by vasopressin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by vasopressin biological process from the curated GO Biological Process Annotations dataset.

regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

detection of hypoxic conditions in blood by carotid body chemoreceptor signaling Gene Set

From GO Biological Process Annotations

genes participating in the detection of hypoxic conditions in blood by carotid body chemoreceptor signaling biological process from the curated GO Biological Process Annotations dataset.

vasodilation by angiotensin involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by angiotensin involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by atrial natriuretic peptide Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by atrial natriuretic peptide biological process from the curated GO Biological Process Annotations dataset.

regulation of blood volume by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood volume by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

negative regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by circulatory renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by circulatory renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, intrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood microparticle formation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood microparticle formation biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by endothelin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by endothelin biological process from the curated GO Biological Process Annotations dataset.

activation of blood coagulation via clotting cascade Gene Set

From GO Biological Process Annotations

genes participating in the activation of blood coagulation via clotting cascade biological process from the curated GO Biological Process Annotations dataset.

regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

angiotensin catabolic process in blood Gene Set

From GO Biological Process Annotations

genes participating in the angiotensin catabolic process in blood biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by hormone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by hormone biological process from the curated GO Biological Process Annotations dataset.

detection of hypoxic conditions in blood by chemoreceptor signaling Gene Set

From GO Biological Process Annotations

genes participating in the detection of hypoxic conditions in blood by chemoreceptor signaling biological process from the curated GO Biological Process Annotations dataset.

blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the blood circulation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

neurological system process involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the neurological system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by ischemic conditions Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by ischemic conditions biological process from the curated GO Biological Process Annotations dataset.

phosphatidylserine exposure on blood platelet Gene Set

From GO Biological Process Annotations

genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations dataset.

lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations dataset.

regulation of lung blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lung blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by baroreceptor feedback Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by baroreceptor feedback biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, common pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, common pathway biological process from the curated GO Biological Process Annotations dataset.

vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

renal system process involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

blood microparticle Gene Set

From GO Cellular Component Annotations

proteins localized to the blood microparticle cellular component from the curated GO Cellular Component Annotations dataset.

blood Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in blood relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

Blood pressure measurement (high sodium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Diastolic blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Diastolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Triglycerides-Blood Pressure (TG-BP) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Triglycerides-Blood Pressure (TG-BP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (cold pressor test) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Diastolic blood pressure (alcohol consumption interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White blood cell types Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell types phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red blood cell traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure in sickle cell anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (high sodium and potassium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood metabolite levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood metabolite levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure (age interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

C-reactive protein and white blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Obesity and blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity and blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Se levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Se levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood metabolite ratios Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood metabolite ratios phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (low sodium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure (alcohol consumption interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Zn levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Zn levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Cu levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Cu levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

blood protein disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood protein disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

blood platelet disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood platelet disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

blood coagulation disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

inherited blood coagulation disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease inherited blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

increased blood urea nitrogen (bun) Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased blood urea nitrogen (bun) phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

elevated systolic blood pressure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the elevated systolic blood pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-to-normal blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the low-to-normal blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased blood urea nitrogen (bun) Gene Set

From HPO Gene-Disease Associations

genes associated with the increased blood urea nitrogen (bun) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated diastolic blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated diastolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent microvilli on the surface of peripheral blood lymphocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the absent microvilli on the surface of peripheral blood lymphocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated systolic blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated systolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prolonged whole-blood clotting time Gene Set

From HPO Gene-Disease Associations

genes associated with the prolonged whole-blood clotting time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prominent superficial blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the prominent superficial blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red blood cell mass Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red blood cell mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of blood circulation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood circulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Blood Loss, Surgical Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Loss, Surgical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Coagulation Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Coagulation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Platelet Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Platelet Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Coagulation Disorders, Inherited Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Coagulation Disorders, Inherited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Group Incompatibility Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Group Incompatibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood group Rhesus C/E/D polypeptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood group Rhesus C/E/D polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Blood coagulation inhibitor, Disintegrin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood coagulation inhibitor, Disintegrin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kell blood group glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kell blood group glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

decreased blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent visceral yolk sac blood islands Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent visceral yolk sac blood islands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial systolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mean systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial diastolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mean systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vitelline blood vessels Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vitelline blood vessels phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial systolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial diastolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[blood group, swann] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, swann] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rodgers] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rodgers] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, colton] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, colton] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, knops system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, knops system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[junior blood group system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [junior blood group system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, raph] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, raph] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group gil] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group gil] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, dombrock] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, dombrock] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, waldner] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, waldner] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, scianna system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, scianna system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, mn] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, mn] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, xg system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, xg system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, abo system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, abo system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ok] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ok] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, auberger system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, auberger system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[white blood cell count qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [white blood cell count qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, indian system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, indian system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, froese] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, froese] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, landsteiner-wiener] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, landsteiner-wiener] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rhesus] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rhesus] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, globoside system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, globoside system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran null] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran null] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood pressure regulation qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood pressure regulation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kell] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kell] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, radin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, radin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kidd] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kidd] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, yt system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, yt system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p(k) phenotype] Gene Set