leukoencephalopathy with dystonia and motor neuropathy

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Results for "leukoencephalopathy with dystonia and motor neuropathy": 1002 gene sets

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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.
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.
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.
Leber hereditary optic neuropathy and dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy and dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease 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.
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.
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.
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 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.
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.
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 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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
Hereditary Motor And Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor And Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor And Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hereditary axonal motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
subcortical infarcts and leukoencephalopathy (cadasil)] Gene Set From GAD Gene-Disease Associations genes associated with the disease subcortical infarcts and leukoencephalopathy (cadasil)] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subcortical infarcts and leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease subcortical infarcts and leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease adult-onset leukoencephalopathy with axonal spheroids and pigmented glia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease adult-onset leukoencephalopathy with axonal spheroids and pigmented glia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microangiopathy and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microangiopathy and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
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.
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.
asymmetric motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
distal hereditary motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
motor peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
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.
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.
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.
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.
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, 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.
Peripheral Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hmn (Hereditary Motor Neuropathy) Proximal Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Motor Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Motor Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Hereditary Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Motor Sensory Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Motor Sensory Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Axonal Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Demyelinating Motor Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Demyelinating Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asymmetric motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asymmetric motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal hereditary motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary motor cortex cell_Primary motor cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Primary motor cortex cell_Primary motor cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.
hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene Set From OMIM Gene-Disease Associations genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Leber Optic Atrophy And Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness, dystonia, and cerebral hypomyelination in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegenerative illness progressing to crippling dystonia and death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodegenerative illness progressing to crippling dystonia and death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leukoencephalopathy, progressive, with ovarian failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, progressive, with ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, cystic, without megalencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary diffuse leukoencephalopathy with spheroids Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary diffuse leukoencephalopathy with spheroids phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with vanishing white matter Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with vanishing white matter phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy With Metaphyseal Chondrodysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy With Metaphyseal Chondrodysplasia from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Megalencephalic leukoencephalopathy with subcortical cysts from the curated CTD Gene-Disease Associations dataset.
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.
Posterior Leukoencephalopathy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Posterior Leukoencephalopathy Syndrome from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Progressive Multifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Progressive Multifocal from the curated CTD Gene-Disease Associations dataset.
progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
stroke, lacunar; leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral arteriopathy; leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral arteriopathy; leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukoencephalopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term leukoencephalopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the posterior leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse spongiform leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse spongiform leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2a Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, diffuse hereditary, with spheroids Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, diffuse hereditary, with spheroids phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with vanishing white matter Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, progressive, with ovarian failure Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, progressive, with ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with metaphyseal chondrodysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with metaphyseal chondrodysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, cystic, without megalencephaly Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
Hereditary Diffuse Leukoencephalopathy With Spheroids Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Diffuse Leukoencephalopathy With Spheroids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Megalencephalic Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Megalencephalic Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Vascular Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Vascular Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cavitating Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cavitating Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Leukoencephalopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Leukoencephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Spongiform Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Spongiform Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leukoencephalopathy with vanishing white matter Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leukoencephalopathy with vanishing white matter from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
RNASET2-deficient cystic leukoencephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease RNASET2-deficient cystic leukoencephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Megalencephalic leukoencephalopathy with subcortical cysts from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukoencephalopathy with vanishing white matter Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukoencephalopathy with vanishing white matter in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive leukoencephalopathy with ovarian failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive leukoencephalopathy with ovarian failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
RNASET2-deficient cystic leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease RNASET2-deficient cystic leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypomyelinating leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypomyelinating leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukoencephalopathy with vanishing white matter 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leukoencephalopathy with vanishing white matter 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Megalencephalic leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Megalencephalic leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary diffuse leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary diffuse leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cystic leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
inflammatory and toxic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
?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.
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, 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.
?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.
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.
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.
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.
?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.
Peripheral Neuropathy Due To And Following Chemotherapy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy Due To And Following Chemotherapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory And Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory And Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory And Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory And Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary And Idiopathic Neuropathy, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary And Idiopathic Neuropathy, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inflammatory and toxic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensory and autonomic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial dilated cardiomyopathy and peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial dilated cardiomyopathy and peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foot ulcer in diabetes and neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Foot ulcer in diabetes and neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
tic; combined vocal and multiple motor; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Parkinson's disease (motor and cognition) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hereditary Motor and Sensory Neuropathies Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Motor and Sensory Neuropathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Facial Onset Sensory And Motor Neuronopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Onset Sensory And Motor Neuronopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood-onset motor and cognitive regression syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Parkinson's disease (motor and cognition) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Dystonia 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant torsion dystonia 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant torsion dystonia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 6, torsion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 6, torsion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 5, Dopa-responsive type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 5, Dopa-responsive type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 3, torsion, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinsonism-Dystonia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.
Dystonia musculorum deformans type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia musculorum deformans type 2 from the curated CTD Gene-Disease Associations dataset.
Dystonia 13, Torsion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 13, Torsion from the curated CTD Gene-Disease Associations dataset.
Dystonia musculorum deformans type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia musculorum deformans type 1 from the curated CTD Gene-Disease Associations dataset.
Torsion dystonia 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Torsion dystonia 7 from the curated CTD Gene-Disease Associations dataset.
Dystonia 17, Torsion, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 17, Torsion, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Dystonia 15, myoclonic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 15, myoclonic from the curated CTD Gene-Disease Associations dataset.
Dystonia 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 12 from the curated CTD Gene-Disease Associations dataset.
Myoclonic dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic dystonia from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.
Juvenile-onset dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile-onset dystonia from the curated CTD Gene-Disease Associations dataset.
Dystonia 3, Torsion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 3, Torsion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Dystonia 6, torsion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 6, torsion from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-responsive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-responsive from the curated CTD Gene-Disease Associations dataset.
Cervical Dystonia, Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cervical Dystonia, Primary from the curated CTD Gene-Disease Associations dataset.
Dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia from the curated CTD Gene-Disease Associations dataset.
generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease generalized dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
deafness dystonia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease deafness dystonia syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dystonia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease dystonia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranio-facial dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
deafness dystonia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease deafness dystonia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dystonia, primary torsion Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, primary torsion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complex regional pain syndromes; dystonia; Gene Set From GAD Gene-Disease Associations genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myoclonus dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease myoclonus dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia; Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic torsion dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, primary Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cervical dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease cervical dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, cervical Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, cervical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, focal Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, focal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blepharospasm; dystonia; dystonic disorders; torticollis Gene Set From GAD Gene-Disease Associations genes associated with the disease blepharospasm; dystonia; dystonic disorders; torticollis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, early onset primary Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
akathisia, drug-induced; dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease akathisia, drug-induced; dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia; psychomotor disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia; psychomotor disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease focal dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dystonia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Musician's dystonia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
craniofacial dystonia Gene Set From HPO Gene-Disease Associations genes associated with the craniofacial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb dystonia Gene Set From HPO Gene-Disease Associations genes associated with the limb dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized dystonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axial dystonia Gene Set From HPO Gene-Disease Associations genes associated with the axial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
oromandibular dystonia Gene Set From HPO Gene-Disease Associations genes associated with the oromandibular dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dystonia Gene Set From HPO Gene-Disease Associations genes associated with the dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
paroxysmal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the paroxysmal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
torsion dystonia Gene Set From HPO Gene-Disease Associations genes associated with the torsion dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the focal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Dystonia Musculorum Deformans Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dystonia Musculorum Deformans phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dystonia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dystonia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
dystonia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dystonia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dystonia 6, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 6, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-17, primary torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-17, primary torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-parkinsonism, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 4, torsion, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 4, torsion, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 9 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 13, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 13, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-12 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 21 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 24 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 25 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, primary cervical Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, primary cervical phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-1, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-1, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
{dystonia-1, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {dystonia-1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinsonism-dystonia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-7, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-7, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-11, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-11, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, juvenile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-15, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-15, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 16 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, early-onset atypical, with myoclonic features Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.
Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile-Onset Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile-Onset Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Musician'S Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Musician'S Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Segmental Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Segmental Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dopa-Responsive Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dopa-Responsive Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cervical Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Cervical Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fragments Of Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fragments Of Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Dystonia, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Dystonia, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngeal Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniofacial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniofacial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Oromandibular Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oromandibular Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lingual Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lingual Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axial Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acute Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leg Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leg Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
dystonia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dystonia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 pathway from the Reactome Pathways 2024 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 pathway from the Reactome Pathways 2024 dataset.
Dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Focal dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Focal dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked dystonia-parkinsonism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Torsion dystonia 6 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Torsion dystonia 6 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
dystonia, DOPA-responsive Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease dystonia, DOPA-responsive from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dystonia 12 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia 12 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dystonia 16 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia 16 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multifocal dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multifocal dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease deafness-dystonia-optic neuronopathy syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hypermanganesemia with dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness-dystonia-optic neuronopathy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal hand dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal hand dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multifocal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multifocal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oromandibular dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oromandibular dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Segmental dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Segmental dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile parkinsonism-dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile parkinsonism-dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spasmodic dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spasmodic dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cervical dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervical dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dystonia-parkinsonism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 28, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
dystonia, DOPA-responsive Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dystonia, DOPA-responsive in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 35, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cranio-facial dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Torsion dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Paroxysmal dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Paroxysmal dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset generalized limb-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset generalized limb-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive DOPA responsive dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive DOPA responsive dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dopa-responsive dystonia due to sepiapterin reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia due to sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental malformations-deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental malformations-deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dopa-responsive dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonus-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonus-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked dystonia-parkinsonism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Deafness dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Deafness dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TSPOAP1-related Dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TSPOAP1-related Dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Musician's dystonia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease Association 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 Association 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 Association 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 Association 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 Association 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 Association 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.
autonomic peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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 Association 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 Association 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.
toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
sensory peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
diabetic autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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.
leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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.
anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
median neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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.
ischemic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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.
diabetic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
{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.
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.
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.
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, 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.
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.
Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tangier Disease Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tangier Disease Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Fiber Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Fiber Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sciatic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sciatic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorimotor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorimotor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arteritic Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arteritic Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcoholic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcoholic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculitic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculitic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Axonal Sensorimotor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axonal Sensorimotor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unspecified Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unspecified Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Constrictive Median Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Constrictive Median Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Neuropathy, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Neuropathy, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Mag Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Mag Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giant Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giant Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy, Ischemic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy, Ischemic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypomyelinating Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypomyelinating Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Neuropathy Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Neuropathy Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Length-Dependent Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Length-Dependent Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giant Axonal Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giant Axonal Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Peripheral Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory Radicular Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Radicular Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dejerine-Sottas Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dejerine-Sottas Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Arteritic Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Arteritic Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Polyglucosan Body Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Polyglucosan Body Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Median Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Median Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Demyelinating Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Demyelinating Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominantly Inherited Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominantly Inherited Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hollow Visceral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hollow Visceral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensory Axonal Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensory Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensory Ataxic Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensory Ataxic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Auditory Neuropathy, Nonsyndromic Recessive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Auditory Neuropathy, Nonsyndromic Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
optic neuropathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic neuropathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Intracellular trafficking proteins involved in CMT neuropathy Gene Set From WikiPathways Pathways 2024 proteins participating in the Intracellular trafficking proteins involved in CMT neuropathy pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) pathway from the Reactome Pathways 2024 dataset.
Neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leber hereditary optic neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia with axonal neuropathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Brachial plexus neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Brachial plexus neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Agenesis of the corpus callosum with peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Agenesis of the corpus callosum with peripheral neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary neuropathy with liability to pressure palsies Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary neuropathy with liability to pressure palsies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1E Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy type 1E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuropathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Neuropathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Axonal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Axonal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tibial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tibial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brachial plexus neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brachial plexus neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary neuropathy with liability to pressure palsies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary neuropathy with liability to pressure palsies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Toxic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sensory peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant auditory neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant auditory neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sciatic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sciatic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nutritional optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nutritional optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uremic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uremic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alcoholic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcoholic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroneal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroneal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Agenesis of the corpus callosum with peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Agenesis of the corpus callosum with peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ulnar neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ulnar neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ischemic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ischemic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Radial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Radial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Femoral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Median neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Median neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic peripheral autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic peripheral autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Giant axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Giant axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Giant axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Giant axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult polyglucosan body neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult polyglucosan body neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonarteritic anterior ischemic optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonarteritic anterior ischemic optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensorimotor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensorimotor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Giant axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Giant axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataracts-facial dysmorphism-neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataracts-facial dysmorphism-neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensory ataxic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory ataxic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dejerine-sottas neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dejerine-sottas neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sensory neuropathy-deafness-dementia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensory neuropathy-deafness-dementia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Demyelinating peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Demyelinating peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Small fiber neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Small fiber neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive demyelinating neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive demyelinating neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visceral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sensorimotor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensorimotor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GARS-Associated Axonal Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GARS-Associated Axonal Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia Neuropathy Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia Neuropathy Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant auditory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber-like hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber-like hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital hypomyelination neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hypomyelination neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diabetic neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neuropathy x type 2 diabetes interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuropathy x type 2 diabetes interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic peripheral neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic peripheral neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Paclitaxel-induced neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 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 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 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 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 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 2025 dataset.
Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Taxane-induced peripheral neuropathy in breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Taxane-induced peripheral neuropathy in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia 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.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
facial motor nucleus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in facial motor nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
motor nucleus of trigeminal nerve, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in motor nucleus of trigeminal nerve, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
motor nucleus of trigeminal nerve, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in motor nucleus of trigeminal nerve, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
dorsal motor nucleus of the vagus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal motor nucleus of the vagus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
facial motor nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in facial motor nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
dorsal motor nucleus of the vagus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal motor nucleus of the vagus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, intermediate white layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r7 portion of ambiguous motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r7 portion of ambiguous motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r9 portion of vagal motor nucleus (postmigratory) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 portion of vagal motor nucleus (postmigratory) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Motor nucleus of trigeminal Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Motor nucleus of trigeminal relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r10 part of vagal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 part of vagal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
anterior digastric muscle trigeminal motor cell group Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, deep white layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, deep white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r3 part of the trigeminal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r3 part of the trigeminal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area, Layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area, Layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Facial motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Facial motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r7 portion of the hypoglossal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r7 portion of the hypoglossal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area, Layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r2 part of the trigeminal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r2 part of the trigeminal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
temporal muscle trigeminal motor cell group Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in temporal muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area, Layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary motor area, Layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Midbrain, motor related Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Midbrain, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r9 portion of ambiguous motor nucleus (postmigratory) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 portion of ambiguous motor nucleus (postmigratory) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, deep gray layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, deep gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r8 portion of the hypoglossal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r8 portion of the hypoglossal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
abducens motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in abducens motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r8 portion of ambiguous motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r8 portion of ambiguous motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, intermediate gray layer, sublayer a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, intermediate gray layer, sublayer c Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer c relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, intermediate gray layer, sublayer b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Accessory facial motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Accessory facial motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Pons, motor related Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pons, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Thalamus, sensory-motor cortex related Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Thalamus, sensory-motor cortex related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, motor related, intermediate gray layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
pterigoid muscle trigeminal motor cell group Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in pterigoid muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Dorsal motor nucleus of the vagus nerve Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Dorsal motor nucleus of the vagus nerve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
temporotympanic muscle trigeminal motor cell group Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in temporotympanic muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r9 portion of the hypoglossal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 portion of the hypoglossal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Medulla, motor related Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medulla, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r10 portion of the hypoglossal motor nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 portion of the hypoglossal motor nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
primary motor cortex (area M1, area 4)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor-sensory cortex (samples)_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary motor cortex (area M1, area 4)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor-sensory cortex (samples)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor-sensory cortex (samples)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_4 mos_M_12889 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor-sensory cortex (samples)_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor-sensory cortex (samples)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor cortex (area M1, area 4)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary motor-sensory cortex (samples)_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
dorsal motor nucleus of the vagus (vagal nucleus) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal motor nucleus of the vagus (vagal nucleus) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in posterior frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in posterior frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
motor nucleus of trigeminal nerve Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in motor nucleus of trigeminal nerve relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in posteror frontal cortex (motor cortex) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Distal hereditary motor neuronopathy 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 5B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
presequence translocase-associated import motor Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the presequence translocase-associated import motor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Neuronopathy, Distal Hereditary Motor, Type V Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset.
Neuronopathy, Distal Hereditary Motor, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset.
Motor Neuron Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset.
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset.
Motor Skills Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Motor Skills Disorders from the curated CTD Gene-Disease Associations dataset.
Neuronopathy, Distal Hereditary Motor, Type Viib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset.
motor neuron disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease motor neuron disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
motor neuron disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease motor neuron disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
motor neuron disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease motor neuron disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial motor epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial motor epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
motor neuritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease motor neuritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rapid motor decline Gene Set From GAD Gene-Disease Associations genes associated with the disease rapid motor decline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sporadic adult-onset lower motor neuron disease Gene Set From GAD Gene-Disease Associations genes associated with the disease sporadic adult-onset lower motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor neuron disease; paraparesis, spastic Gene Set From GAD Gene-Disease Associations genes associated with the disease motor neuron disease; paraparesis, spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function; motor function Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function; motor function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor neuron disease Gene Set From GAD Gene-Disease Associations genes associated with the disease motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bulbar-onset motor neuron disease Gene Set From GAD Gene-Disease Associations genes associated with the disease bulbar-onset motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor unit response Gene Set From GAD Gene-Disease Associations genes associated with the disease motor unit response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia; dementia; motor neuron disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia; dementia; motor neuron disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
motor Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term motor in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Peripheral motor neuropathy_Sciatic Nerve_GSE1947 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Peripheral motor neuropathy_Sciatic Nerve_GSE1947 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
smoothened signaling pathway involved in spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of lateral motor column neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
somatic motor neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the somatic motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
medial motor column neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the medial motor column neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of microtubule motor activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of microtubule motor activity biological process from the curated GO Biological Process Annotations 2015 dataset.
lateral motor column neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
fasciculation of motor neuron axon Gene Set From GO Biological Process Annotations 2015 genes participating in the fasciculation of motor neuron axon biological process from the curated GO Biological Process Annotations 2015 dataset.
motor neuron axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the motor neuron axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in somatic motor neuron fate commitment Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in somatic motor neuron fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of microtubule motor activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of microtubule motor activity biological process from the curated GO Biological Process Annotations 2015 dataset.
visceral motor neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the visceral motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
motor neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the motor neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of lateral motor column neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
presequence translocase-associated import motor Gene Set From GO Cellular Component Annotations 2015 proteins localized to the presequence translocase-associated import motor cellular component from the curated GO Cellular Component Annotations 2015 dataset.
microfilament motor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the microfilament motor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
minus-end directed microfilament motor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the minus-end directed microfilament motor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
plus-end directed microfilament motor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the plus-end directed microfilament motor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
microtubule motor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the microtubule motor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
motor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the motor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
atp-dependent microtubule motor activity, plus-end-directed Gene Set From GO Molecular Function Annotations 2015 genes performing the atp-dependent microtubule motor activity, plus-end-directed molecular function from the curated GO Molecular Function Annotations 2015 dataset.
atp-dependent microtubule motor activity, minus-end-directed Gene Set From GO Molecular Function Annotations 2015 genes performing the atp-dependent microtubule motor activity, minus-end-directed molecular function from the curated GO Molecular Function Annotations 2015 dataset.
motor neuron disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease motor neuron disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of central motor function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal motor neuron morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
motor neuron atrophy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of extrapyramidal motor function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal motor seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the focal motor seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal motor nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor deterioration Gene Set From HPO Gene-Disease Associations genes associated with the motor deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal upper motor neuron morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
functional motor problems Gene Set From HPO Gene-Disease Associations genes associated with the functional motor problems phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor delay Gene Set From HPO Gene-Disease Associations genes associated with the motor delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor tics Gene Set From HPO Gene-Disease Associations genes associated with the motor tics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of extrapyramidal motor function Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of extrapyramidal motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor aphasia Gene Set From HPO Gene-Disease Associations genes associated with the motor aphasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor neuron atrophy Gene Set From HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal lower motor neuron morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed gross motor development Gene Set From HPO Gene-Disease Associations genes associated with the delayed gross motor development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal motor seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal motor seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of central motor function Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of central motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cranial nerve motor loss Gene Set From HPO Gene-Disease Associations genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
poor gross motor coordination Gene Set From HPO Gene-Disease Associations genes associated with the poor gross motor coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
paucity of anterior horn motor neurons Gene Set From HPO Gene-Disease Associations genes associated with the paucity of anterior horn motor neurons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
poor motor coordination Gene Set From HPO Gene-Disease Associations genes associated with the poor motor coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal motor neuron morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased motor nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor polyneuropathy Gene Set From HPO Gene-Disease Associations genes associated with the motor polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
poor fine motor coordination Gene Set From HPO Gene-Disease Associations genes associated with the poor fine motor coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Motor Skills Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Motor Skills phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Motor Skills Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Motor Skills Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Motor Neuron Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Motor Neuron Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Kinesin motor domain, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinesin motor domain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kinesin motor domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinesin motor domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Survival motor neuron Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Survival motor neuron protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Harmonizome 3.0

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

leukoencephalopathy with dystonia and motor neuropathy Gene Set

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

Leber hereditary optic neuropathy and dystonia Gene Set

Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Gene Set

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

X-linked hereditary motor and sensory neuropathy Gene Set

Hereditary Sensory and Motor Neuropathy Gene Set

Neuropathy, hereditary motor and sensory, Russe type Gene Set

Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set

Hereditary Motor And Sensory Neuropathy VI Gene Set

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

Neuropathy, hereditary motor and sensory, LOM type Gene Set

neuropathy, hereditary motor and sensory Gene Set

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

Hereditary Sensory and Motor Neuropathy Gene Set

neuropathy, motor and sensory, russe type Gene Set

hereditary motor and sensory neuropathy v Gene Set

neuropathy, hereditary motor and sensory, russe type Gene Set

hereditary motor and sensory neuropathy, proximal type Gene Set

hereditary motor and sensory neuropathy, type iic Gene Set

hereditary motor and sensory neuropathy vi Gene Set

Hereditary Motor And Sensory Neuropathy Gene Set

Motor And Sensory Neuropathy Gene Set

Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene Set

Hereditary motor and sensory neuropathy Gene Set

Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

subcortical infarcts and leukoencephalopathy (cadasil)] Gene Set

subcortical infarcts and leukoencephalopathy Gene Set

White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Gene Set

adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Gene Set

adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Gene Set

Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Gene Set

Microangiopathy and leukoencephalopathy Gene Set

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

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

Neuropathy, Distal Hereditary Motor, Type IIA Gene Set

Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set

asymmetric motor neuropathy Gene Set

distal hereditary motor neuropathy Gene Set

motor peripheral neuropathy Gene Set

demyelinating motor neuropathy Gene Set

motor axonal neuropathy Gene Set

neuropathy, distal hereditary motor, jerash type Gene Set

neuropathy, distal hereditary motor, type va Gene Set

neuropathy, distal hereditary motor, type viib Gene Set

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

neuropathy, distal hereditary motor, type iib Gene Set

neuropathy, distal hereditary motor, type iia Gene Set

Peripheral Motor Neuropathy Gene Set

Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene Set

Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene Set

Asymmetric Diabetic Proximal Motor Neuropathy Gene Set

Symmetric Diabetic Proximal Motor Neuropathy Gene Set

Multifocal Motor Neuropathy Gene Set

Acute Motor Axonal Neuropathy Gene Set

Distal Hereditary Motor Neuropathy Gene Set

Acute Motor Sensory Axonal Neuropathy Gene Set

Motor Axonal Neuropathy Gene Set

Demyelinating Motor Neuropathy Gene Set

Motor peripheral neuropathy Gene Set

Asymmetric motor neuropathy Gene Set

Distal hereditary motor neuropathy Gene Set

Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set

Peripheral motor neuropathy Gene Set

Primary motor cortex cell_Primary motor cortex_Mouse Gene Set

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set

deafness, dystonia, and cerebral hypomyelination Gene Set

epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set