Name

Optic Neuropathy, Ischemic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Neuropathy, Ischemic from the curated CTD Gene-Disease Associations dataset.

Optic Neuropathy, Ischemic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Neuropathy, Ischemic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

anterior ischemic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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.

atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; optic neuropathy, ischemic Gene Set

From GAD Gene-Disease Associations

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

nonarteritic anterior ischemic optic neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{nonarteritic anterior ischemic optic neuropathy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nonarteritic anterior ischemic optic neuropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; ischemic attack, transient; obesity; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; ischemic attack, transient; obesity; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; diabetes mellitus; ischemic attack, transient; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; diabetes mellitus; ischemic attack, transient; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.

toxic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

leber hereditary optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

leber's hereditary optic neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leber's hereditary optic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic neuropathy Gene Set

From HPO Gene-Disease Associations

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

optic neuropathy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic neuropathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spastic paraplegia, optic atrophy, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced Gene Set

From CORUM Protein Complexes

proteins in the Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced protein complex from the CORUM Protein Complexes dataset.

Ischemic Attack, Transient Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ischemic Attack, Transient from the curated CTD Gene-Disease Associations dataset.

Colitis, Ischemic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Colitis, Ischemic from the curated CTD Gene-Disease Associations dataset.

ischemic bone disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

ischemic bone disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

ischemic bone disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ischemic fasciitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disease, ischemic; fibrinogen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disease, ischemic; fibrinogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis, ischemic; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ischemic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; lipoprotein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; atherosclerosis, coronary; hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; atherosclerosis, coronary; hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

cardiovascular disease; stroke; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; thromboembolism, venous; c-reactive protein; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; thromboembolism, venous; c-reactive protein; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic cerebrovascular diseases Gene Set

From GAD Gene-Disease Associations

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

cerebral ischemic events Gene Set

From GAD Gene-Disease Associations

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

stroke, ischemic; cerebrovascular disease; thrombosis, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke, ischemic; cerebrovascular disease; thrombosis, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic and ischemic stroke Gene Set

From GAD Gene-Disease Associations

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

stroke, ischemic; atherosclerosis, carotid Gene Set

From GAD Gene-Disease Associations

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

cognitive impairment, vascular stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cognitive impairment, vascular stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; heart disease, ischemic; diabetes, type 2; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; heart disease, ischemic; diabetes, type 2; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; hypertension; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; hypertension; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain hemorrhage; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain hemorrhage; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke, ischemic; stroke, hemorrhagic Gene Set

From GAD Gene-Disease Associations

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

early onset ischemic heart disease. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset ischemic heart disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; ischemic attack, transient; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; ischemic attack, transient; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

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

stroke, ischemic; fibrinogen Gene Set

From GAD Gene-Disease Associations

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

intracranial arteriosclerosis; ischemic attack, transient; myocardial infarction; recurrence; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial arteriosclerosis; ischemic attack, transient; myocardial infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; insulin Gene Set

From GAD Gene-Disease Associations

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

stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

hypertension; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis, coronary; diabetes, type 2; lipids; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; diabetes, type 2; lipids; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic neuronal cell death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ischemic neuronal cell death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolism disorders; myocardial infarction; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

ischemic stroke Gene Set

From GAD Gene-Disease Associations

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

ischemic coronary and cerebrovascular events Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; c-reactive protein; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; c-reactive protein; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic Gene Set

From GeneRIF Biological Term Annotations

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

ischemicnecrotic Gene Set

From GeneRIF Biological Term Annotations

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

ischemicidiopathic Gene Set

From GeneRIF Biological Term Annotations

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

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.

Ischemic stroke Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Coronary artery disease or ischemic stroke Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary artery disease or ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Stroke (ischemic) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Stroke (ischemic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

ischemic bone disease Gene Set

From GWASdb SNP-Disease Associations

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

ischemic stroke Gene Set

From GWASdb SNP-Phenotype Associations

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

transient ischemic attack Gene Set

From HPO Gene-Disease Associations

genes associated with the transient ischemic attack phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ischemic stroke Gene Set

From HPO Gene-Disease Associations

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

Ischemic Attack, Transient Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ischemic Attack, Transient phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Colitis, Ischemic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

increased time of peak ischemic contracture Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased time of peak ischemic contracture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered response to cns ischemic injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered response to cns ischemic injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{stroke, ischemic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stroke, ischemic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{ischemic stroke, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {ischemic stroke, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

ischemic Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term ischemic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

lateral terminal nucleus of the accessory optic tract, lateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral terminal nucleus of the accessory optic tract, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral terminal nucleus of the accessory optic tract, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral terminal nucleus of the accessory optic tract, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

dorsal terminal nucleus of the accessory optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsal terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, optic layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, optic layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Nucleus of the optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Nucleus of the optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral terminal nucleus of the accessory optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

optic fiber layer of SC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in optic fiber layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dominant hereditary optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic Atrophy Type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma of optic disc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma of optic disc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve hypoplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve aplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Septo-optic dysplasia sequence Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic Neuritis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Neuritis from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Hereditary, Leber Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset.

Optic Atrophies, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.

Optic Nerve Hypoplasia, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.

Polymicrogyria With Optic Nerve Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Costeff optic atrophy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.

Optic atrophy polyneuropathy deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Optic Nerve Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Nerve Diseases from the curated CTD Gene-Disease Associations dataset.

Cavitary Optic Disc Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cavitary Optic Disc Anomalies from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.

Coloboma of optic nerve Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coloboma of optic nerve from the curated CTD Gene-Disease Associations dataset.

OPTIC ATROPHY 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Optic Disk Gene Set

From dbGAP Gene-Trait Associations

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

Optic Nerve Gene Set

From dbGAP Gene-Trait Associations

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

optic nerve disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

primary optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic papillitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic disk drusen Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic neuritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve sheath meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease optic nerve sheath meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

optic nerve glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple sclerosis; optic neuritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic disc atrophy Gene Set

From GAD Gene-Disease Associations

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

optic atrophy Gene Set

From GAD Gene-Disease Associations

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

optic nerve diseases Gene Set

From GAD Gene-Disease Associations

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

blindness; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic disk Gene Set

From GAD Gene-Disease Associations

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

optic nerve Gene Set

From GAD Gene-Disease Associations

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

cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic nerve malformation Gene Set

From GAD Gene-Disease Associations

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

optic atrophy and moderate deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic Gene Set

From GeneRIF Biological Term Annotations

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

optic nerve development Gene Set

From GO Biological Process Annotations

genes participating in the optic nerve development biological process from the curated GO Biological Process Annotations dataset.

optic nerve morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the optic nerve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

optic vesicle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the optic vesicle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

optic placode formation Gene Set

From GO Biological Process Annotations

genes participating in the optic placode formation biological process from the curated GO Biological Process Annotations dataset.

optic cup morphogenesis involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of optic nerve formation Gene Set

From GO Biological Process Annotations

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

regulation of optic nerve formation Gene Set

From GO Biological Process Annotations

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

optic cup structural organization Gene Set

From GO Biological Process Annotations

genes participating in the optic cup structural organization biological process from the curated GO Biological Process Annotations dataset.

optic nerve structural organization Gene Set

From GO Biological Process Annotations

genes participating in the optic nerve structural organization biological process from the curated GO Biological Process Annotations dataset.

closure of optic fissure Gene Set

From GO Biological Process Annotations

genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations dataset.

optic cup formation involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

optic placode formation involved in camera-type eye formation Gene Set

From GO Biological Process Annotations

genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations dataset.

optic chiasma development Gene Set

From GO Biological Process Annotations

genes participating in the optic chiasma development biological process from the curated GO Biological Process Annotations dataset.

Optic nerve measurement (rim area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (rim area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (disc area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (disc area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup-to-disc ratio) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup-to-disc ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic disc parameters Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic disc parameters phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

optic nerve disease Gene Set

From GWASdb SNP-Disease Associations

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

optic nerve coloboma Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic disc hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic atrophy Gene Set

From HPO Gene-Disease Associations

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

optic disc drusen Gene Set

From HPO Gene-Disease Associations

genes associated with the optic disc drusen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the optic disc Gene Set

From HPO Gene-Disease Associations

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

optic disc pallor Gene Set

From HPO Gene-Disease Associations

genes associated with the optic disc pallor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

leber optic atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic atrophy from cranial nerve compression Gene Set

From HPO Gene-Disease Associations

genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve compression Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retrobulbar optic neuritis Gene Set

From HPO Gene-Disease Associations

genes associated with the retrobulbar optic neuritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

septo-optic dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic glioma Gene Set

From HPO Gene-Disease Associations

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

optic neuritis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the optic nerve Gene Set

From HPO Gene-Disease Associations

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

Optic Neuritis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Neuritis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Septo-Optic Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophies, Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Nerve Glioma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Nerve Glioma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Disk Drusen Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Disk Drusen phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy, Hereditary, Leber Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Nerve Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Nerve Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic atrophy 3-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal optic disc morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic stalk morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic tract Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic tract phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic placodes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic placodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve coloboma Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic tract morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic placode morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic nerve innervation Gene Set

From MPO Gene-Phenotype Associations

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

absent optic nerve Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic nerve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic nerve morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic cup morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic chiasm morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve swelling Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve swelling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic vesicle formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic vesicle formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic fissure morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic vesicle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic vesicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve cupping Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve cupping phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic disc Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic disc phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged optic nerve Gene Set

From MPO Gene-Phenotype Associations

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

optic disc coloboma Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic disc coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic choroid morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic eminence morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic chiasm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent optic chiasm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic pit morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic atrophy 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia and abnormalities of the central nervous system Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cavitary optic disc anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavitary optic disc anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 3 with cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma of optic nerve Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma of optic nerve phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria with optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria with optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

?neurodegeneration with optic atrophy, childhood onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy plus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{leber optic atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

optic cup Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic nerve Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Giant axonal neuropathy, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Giant axonal neuropathy, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Auditory neuropathy, autosomal recessive, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia autosomal recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Giant axonal neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Giant axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Russe type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Distal Hereditary Motor, Type IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset.

Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Sciatic Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sciatic Neuropathy from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor And Sensory Neuropathy VI Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.

Tomaculous neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tomaculous neuropathy from the curated CTD Gene-Disease Associations dataset.

Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.

46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.

Giant Axonal Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Giant Axonal Neuropathy from the curated CTD Gene-Disease Associations dataset.

Auditory Neuropathy, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, LOM type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset.

Inherited Peripheral Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inherited Peripheral Neuropathy from the curated CTD Gene-Disease Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.

peripheral neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

brachial plexus neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease brachial plexus neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

hereditary sensory neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

brachial plexus neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary sensory neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

inflammatory and toxic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease inflammatory and toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autonomic peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sciatic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcoholic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tibial neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sensory peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

asymmetric motor neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diabetic autonomic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

uremic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

femoral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

distal hereditary motor neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

axonal neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peroneal neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

median neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

radial neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

motor peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diabetic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autonomic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ulnar neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neuropathy, hereditary motor and sensory Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy type 1b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth neuropathy type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetic neuropathy Gene Set

From GAD Gene-Disease Associations

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

charcot-marie-tooth neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy, charcot-marie-tooth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, charcot-marie-tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy, alzheimer's disease related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, alzheimer's disease related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy Gene Set

From GAD Gene-Disease Associations

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

neuropathy, diabetic Gene Set

From GAD Gene-Disease Associations

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

alcohol-related polyneuropathy; alcoholic neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related polyneuropathy; alcoholic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; neuropathy Gene Set

From GAD Gene-Disease Associations

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

neuropathy, small fiber Gene Set

From GAD Gene-Disease Associations

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

dejerine-sottas neuropathy Gene Set

From GAD Gene-Disease Associations

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

neuropathy Gene Set

From GeneRIF Biological Term Annotations

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

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Paclitaxel-induced neuropathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

peripheral neuropathy Gene Set

From GWASdb SNP-Disease Associations

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

sensory peripheral neuropathy Gene Set

From GWASdb SNP-Disease Associations

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

neuropathy Gene Set

From GWASdb SNP-Disease Associations

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

peripheral neuropathy Gene Set

From GWASdb SNP-Phenotype Associations

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

sensory neuropathy Gene Set

From GWASdb SNP-Phenotype Associations

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

sensory axonal neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the sensory axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic axonal neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral axonal neuropathy Gene Set

From HPO Gene-Disease Associations

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

demyelinating motor neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the demyelinating motor neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

motor axonal neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the motor axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

demyelinating peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

sensory ataxic neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the sensory ataxic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

entrapment neuropathy Gene Set

From HPO Gene-Disease Associations

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

peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

sensorimotor neuropathy Gene Set

From HPO Gene-Disease Associations

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

constrictive median neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the constrictive median neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodic peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

sensory neuropathy Gene Set

From HPO Gene-Disease Associations

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

distal peripheral sensory neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hereditary Sensory and Motor Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Alcoholic Neuropathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Alcoholic Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Median Neuropathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Median Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

?neuropathy, hereditary sensory and autonomic, type vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?neuropathy, hereditary sensory and autonomic, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, with spastic paraplegia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.

neuromyotonia and axonal neuropathy, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuromyotonia and axonal neuropathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, congenital hypomyelinating, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, congenital hypomyelinating, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, type iic Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

giant axonal neuropathy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the giant axonal neuropathy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, paraneoplastic sensory Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, paraneoplastic sensory phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, motor and sensory, russe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, jerash type Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.

hereditary motor and sensory neuropathy v Gene Set

From OMIM Gene-Disease Associations

genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset.

auditory neuropathy, autosomal dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the auditory neuropathy, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, type ie Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, type id Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, type id phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, type if Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, type if phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, facial dysmorphism, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

agenesis of the corpus callosum with peripheral neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

small fiber neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the small fiber neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary motor and sensory, russe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, autosomal dominant, with peripheral neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hereditary motor and sensory neuropathy, proximal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type va Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.

hereditary motor and sensory neuropathy, type iic Gene Set

From OMIM Gene-Disease Associations

genes associated with the hereditary motor and sensory neuropathy, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, recurrent, with pressure palsies Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, inflammatory demyelinating Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, inflammatory demyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type vii Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hereditary motor and sensory neuropathy vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the hereditary motor and sensory neuropathy vi phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type viib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.

?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy with dystonia and motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, congenital hypomyelinating Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, congenital hypomyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive with axonal neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive with axonal neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

?giant axonal neuropathy 2, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?giant axonal neuropathy 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.

auditory neuropathy, autosomal recessive, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the auditory neuropathy, autosomal recessive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.