Acute Motor Axonal Neuropathy

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Results for "Acute Motor Axonal Neuropathy": 1001 gene sets

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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.
leukemia, erythroblastic, acute; leukemia, megakaryoblastic, acute; leukemia, monocytic, acute; leukemia, myeloid; leukemia, myeloid, acute; leukemia, myelomonocytic, acute; leukemia, promyelocytic, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, erythroblastic, acute; leukemia, megakaryoblastic, acute; leukemia, monocytic, acute; leukemia, myeloid; leukemia, myeloid, acute; leukemia, myelomonocytic, acute; leukemia, promyelocytic, acute in GWAS and other genetic association datasets from the GAD 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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
leukemia, myelocytic, acute; leukemia, myeloid, acute; leukemias, acute myeloblastic Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelocytic, acute; leukemia, myeloid, acute; leukemias, acute myeloblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD 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, 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.
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.
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.
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.
Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary 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.
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.
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.
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.
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.
neuropathy, distal hereditary motor, jerash type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy v Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
neuropathy, distal hereditary motor, type va Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy vi Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type viib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with dystonia and motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
leukemia, myeloid, acute; leukemias, acute myeloblastic Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; leukemias, acute myeloblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heroin dependence; kidney failure, acute; liver failure, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease heroin dependence; kidney failure, acute; liver failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; acute myelogenous leukemia; B cell lymphoma Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease acute lymphocytic leukemia; acute myelogenous leukemia; B cell lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
acute lymphocytic leukemia; acute myelogenous leukemia; chronic myelogenous leukemia Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease acute lymphocytic leukemia; acute myelogenous leukemia; chronic myelogenous leukemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Acute Lung Injury/Acute Respiratory Distress Syndrome (Ards) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Lung Injury/Acute Respiratory Distress Syndrome (Ards) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease, axonal, type 2s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
axonal growth cone Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the axonal growth cone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
axonal spine Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the axonal spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
axonal growth cone Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the axonal growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
axonal spine Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the axonal spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.
axonal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term axonal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mammillothalamic axonal tract development Gene Set From GO Biological Process Annotations 2015 genes participating in the mammillothalamic axonal tract development biological process from the curated GO Biological Process Annotations 2015 dataset.
axonal fasciculation Gene Set From GO Biological Process Annotations 2015 genes participating in the axonal fasciculation biological process from the curated GO Biological Process Annotations 2015 dataset.
axonal growth cone Gene Set From GO Cellular Component Annotations 2015 proteins localized to the axonal growth cone cellular component from the curated GO Cellular Component Annotations 2015 dataset.
axonal spine Gene Set From GO Cellular Component Annotations 2015 proteins localized to the axonal spine cellular component from the curated GO Cellular Component Annotations 2015 dataset.
axonal degeneration/regeneration Gene Set From HPO Gene-Disease Associations genes associated with the axonal degeneration/regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axonal loss Gene Set From HPO Gene-Disease Associations genes associated with the axonal loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
emg: axonal abnormality Gene Set From HPO Gene-Disease Associations genes associated with the emg: axonal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axonal regeneration Gene Set From HPO Gene-Disease Associations genes associated with the axonal regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse axonal swelling Gene Set From HPO Gene-Disease Associations genes associated with the diffuse axonal swelling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
clusters of axonal regeneration Gene Set From HPO Gene-Disease Associations genes associated with the clusters of axonal regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed demyelinating and axonal polyneuropathy Gene Set From HPO Gene-Disease Associations genes associated with the mixed demyelinating and axonal polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axonal dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal axonal transport Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal axonal transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axonal spheroids Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axonal spheroids phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
charcot-marie-toothe disease, axonal, type 2p Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-toothe disease, axonal, type 2p phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2k Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2k phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2n Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2n phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2m Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2m phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 20 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
?charcot-marie-tooth disease, axonal, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the ?charcot-marie-tooth disease, axonal, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, with vocal cord paresis Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, with vocal cord paresis phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth disease, axonal, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth disease, axonal, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
Axonal growth stimulation Gene Set From Reactome Pathways 2014 proteins participating in the Axonal growth stimulation pathway from the Reactome Pathways dataset.
Axonal growth inhibition (RHOA activation) Gene Set From Reactome Pathways 2014 proteins participating in the Axonal growth inhibition (RHOA activation) pathway from the Reactome Pathways dataset.
Mixed Demyelinating And Axonal Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Demyelinating And Axonal Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Axonal Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Emg: Axonal Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Emg: Axonal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Axonal Swelling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Axonal Swelling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration/Regeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration/Regeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Regeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Regeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Polyneuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Clusters Of Axonal Regeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Clusters Of Axonal Regeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
anterograde axonal protein transport Gene Set From GO Biological Process Annotations 2023 genes participating in the anterograde axonal protein transport biological process from the curated GO Biological Process Annotations 2023 dataset.
anterograde axonal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the anterograde axonal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
axonal transport of mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the axonal transport of mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
retrograde axonal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the retrograde axonal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
axonal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the axonal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
axonal fasciculation Gene Set From GO Biological Process Annotations 2023 genes participating in the axonal fasciculation biological process from the curated GO Biological Process Annotations 2023 dataset.
retrograde axonal protein transport Gene Set From GO Biological Process Annotations 2023 genes participating in the retrograde axonal protein transport biological process from the curated GO Biological Process Annotations 2023 dataset.
retrograde axonal transport of mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the retrograde axonal transport of mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
slow axonal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the slow axonal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
anterograde axonal transport of mitochondrion Gene Set From GO Biological Process Annotations 2023 genes participating in the anterograde axonal transport of mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset.
axonal growth cone Gene Set From GO Cellular Component Annotations 2023 proteins localized to the axonal growth cone cellular component from the curated GO Cellular Component Annotations 2023 dataset.
axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal axonal transport Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal axonal transport phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
axonal spheroids Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axonal spheroids phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
axonal transport Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term axonal transport from the SynGO Synaptic Gene Annotations dataset.
anterograde axonal protein transport Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term anterograde axonal protein transport from the SynGO Synaptic Gene Annotations dataset.
anterograde axonal transport Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term anterograde axonal transport from the SynGO Synaptic Gene Annotations dataset.
anterograde axonal transport of neurotransmitter receptor complex Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term anterograde axonal transport of neurotransmitter receptor complex from the SynGO Synaptic Gene Annotations dataset.
axonal transport of messenger ribonucleoprotein complex Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term axonal transport of messenger ribonucleoprotein complex from the SynGO Synaptic Gene Annotations dataset.
Axonal cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Axonal cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Axonal growth inhibition (RHOA activation) Gene Set From Reactome Pathways 2024 proteins participating in the Axonal growth inhibition (RHOA activation) pathway from the Reactome Pathways 2024 dataset.
Axonal growth stimulation Gene Set From Reactome Pathways 2024 proteins participating in the Axonal growth stimulation pathway from the Reactome Pathways 2024 dataset.
anterograde axonal protein transport Gene Set From GO Biological Process Annotations 2025 genes participating in the anterograde axonal protein transport biological process from the curated GO Biological Process Annotations 2025 dataset.
anterograde axonal transport Gene Set From GO Biological Process Annotations 2025 genes participating in the anterograde axonal transport biological process from the curated GO Biological Process Annotations 2025 dataset.
axonal transport of mitochondrion Gene Set From GO Biological Process Annotations 2025 genes participating in the axonal transport of mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset.
retrograde axonal transport Gene Set From GO Biological Process Annotations 2025 genes participating in the retrograde axonal transport biological process from the curated GO Biological Process Annotations 2025 dataset.
axonal transport Gene Set From GO Biological Process Annotations 2025 genes participating in the axonal transport biological process from the curated GO Biological Process Annotations 2025 dataset.
axonal fasciculation Gene Set From GO Biological Process Annotations 2025 genes participating in the axonal fasciculation biological process from the curated GO Biological Process Annotations 2025 dataset.
retrograde axonal protein transport Gene Set From GO Biological Process Annotations 2025 genes participating in the retrograde axonal protein transport biological process from the curated GO Biological Process Annotations 2025 dataset.
retrograde axonal transport of mitochondrion Gene Set From GO Biological Process Annotations 2025 genes participating in the retrograde axonal transport of mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset.
axonal growth cone Gene Set From GO Cellular Component Annotations 2025 proteins localized to the axonal growth cone cellular component from the curated GO Cellular Component Annotations 2025 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.
Charcot-Marie-Tooth disease axonal type 2F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease, axonal type 2W Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease, axonal type 2W in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation 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.
Charcot-Marie-Tooth disease axonal type 2Q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2Z Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2Z in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2S Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2S in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2T Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2P Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2P in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2CC Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2CC in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2U Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2U in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2V Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2V in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2N Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2N in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2K Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2K in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal type 2O Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Charcot-Marie-Tooth disease axonal type 2O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Axonal growth cone Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Axonal growth cone cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Axonal growth cone Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonal growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Leading edge of axonal growth cone Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Leading edge of axonal growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Axonal spine Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonal spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Charcot-Marie-Tooth disease axonal Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease axonal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HSPB1-related axonal neuropathies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HSPB1-related axonal neuropathies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
EMG: axonal abnormality Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EMG: axonal abnormality phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease axonal - Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease axonal - 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.
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auditory neuropathy, autosomal recessive, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
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.
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.
Sciatic Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sciatic Neuropathy from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.
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.
Tomaculous neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tomaculous neuropathy from the curated CTD Gene-Disease Associations dataset.
Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Neuropathy, 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.
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.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.
peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease 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.
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.
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.
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.
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 and autonomic, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the ?neuropathy, hereditary sensory and autonomic, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, with spastic paraplegia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, congenital hypomyelinating, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, congenital hypomyelinating, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ie Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type id Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type id phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type if Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type if phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital cataracts, facial dysmorphism, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
agenesis of the corpus callosum with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
{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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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 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.
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 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 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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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 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 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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Myosin head, motor domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myosin head, motor domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
small trigeminal motor nucleus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small trigeminal motor nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor nerve collateral sprouting Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor nerve collateral sprouting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor coordination/ balance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor coordination/ balance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal somatic motor system morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic motor system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal facial motor nucleus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal facial motor nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased motor neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor capabilities/coordination/movement Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor capabilities/coordination/movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal trigeminal motor nucleus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal motor nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small facial motor nucleus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small facial motor nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord motor column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord lateral motor column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
motor neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased motor neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor neuron innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor neuron morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor learning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor learning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuronopathy, distal hereditary motor, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type vb Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type viia Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type iid Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.
?neuronopathy, distal hereditary motor, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
motor Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term motor in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
motor trigeminal nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue motor trigeminal nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
motor cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue motor cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Motor Neuron Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Clumsiness - Motor Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clumsiness - Motor Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Neuron Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gross Motor Development Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gross Motor Development Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv-1-Associated Cognitive Motor Complex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv-1-Associated Cognitive Motor Complex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Motor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Motor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Sensory-Motor Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sensory-Motor Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Upper Motor Neuron Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Upper Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Motor Neuron Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Motor Neuronopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor Neuronopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Dementia With Motor Neuron Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Dementia With Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Tic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Speech Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Speech Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Motor Neuron Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease 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.
Decreased Motor Nerve Conduction Velocity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Motor Nerve Conduction Velocity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impaired Motor Coordination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Motor Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Fine Motor Coordination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Fine Motor Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Lower Motor Neuron Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lower Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Fine Motor Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Fine Motor Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Motor Coordination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Motor Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Motor Nerve Conduction Velocity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Motor Nerve Conduction Velocity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Functional Motor Deficit Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Motor Deficit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Disturbances Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Disturbances in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Lower-Limb Motor Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lower-Limb Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Oral Motor Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oral Motor Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chronic Motor Or Vocal Tic Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Motor Or Vocal Tic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Paucity Of Anterior Horn Motor Neurons Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paucity Of Anterior Horn Motor Neurons in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gross Motor Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gross Motor Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Motor Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tic, Motor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tic, Motor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Signs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Motor Manifestations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Manifestations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Central Motor Conduction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Motor Conduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Alcohol Withdrawal-Induced Major Motor Seizure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Withdrawal-Induced Major Motor Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cranial Nerve Motor Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Nerve Motor Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Normal Motor Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Normal Motor Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
motor neuron migration Gene Set From GO Biological Process Annotations 2023 genes participating in the motor neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset.
motor neuron axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the motor neuron axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
fasciculation of motor neuron axon Gene Set From GO Biological Process Annotations 2023 genes participating in the fasciculation of motor neuron axon biological process from the curated GO Biological Process Annotations 2023 dataset.
lateral motor column neuron migration Gene Set From GO Biological Process Annotations 2023 genes participating in the lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
motor learning Gene Set From GO Biological Process Annotations 2023 genes participating in the motor learning biological process from the curated GO Biological Process Annotations 2023 dataset.
visceral motor neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the visceral motor neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset.
motor neuron apoptotic process Gene Set From GO Biological Process Annotations 2023 genes participating in the motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron migration Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset.
PAM complex, Tim23 associated import motor Gene Set From GO Cellular Component Annotations 2023 proteins localized to the PAM complex, Tim23 associated import motor cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal facial motor nucleus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal facial motor nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor neuron morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased motor neuron number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased motor neuron number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased motor neuron number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor capabilities/coordination/movement Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor capabilities/coordination/movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor learning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor learning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor coordination/balance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor coordination/balance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small facial motor nucleus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small facial motor nucleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor neuron innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small trigeminal motor nucleus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small trigeminal motor nucleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor nerve collateral sprouting Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor nerve collateral sprouting phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal somatic motor system morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatic motor system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal trigeminal motor nucleus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal trigeminal motor nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord lateral motor column morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal primary motor cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal primary motor cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor neuron dendrite morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron dendrite morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor developmental delay Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased primary motor cortex size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased primary motor cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased primary motor cortex size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased primary motor cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor capabilities/coordination/movement Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal motor capabilities/coordination/movement phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal motor coordination/balance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal motor coordination/balance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal motor learning Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal motor learning phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Human - Motor Cortex - Class - Glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - Glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Class - GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Class - Non-neuronal cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - Non-neuronal cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Astrocyte Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Astrocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Endothelial cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Endothelial cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Layer 6b glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Lamp5+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Lamp5+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - microglia / perivascular macrophage Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - microglia / perivascular macrophage cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - oligodendrocyte Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - oligodendrocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - oligodendrocyte precursor cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - oligodendrocyte precursor cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Pvalb+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Pvalb+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Sncg+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sncg+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Sst+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sst+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - Vip+ GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Vip+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Subclass - vascular lepotomeningeal cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - vascular lepotomeningeal cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FGFR3+ SERPINI2+ Layer 1 astrocyte Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FGFR3+ SERPINI2+ Layer 1 astrocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FGFR3+ AQP1+ Layer 1-6 astrocyte Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FGFR3+ AQP1+ Layer 1-6 astrocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FGFR3+ PLCG1+ Layer 1-6 astrocyte Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FGFR3+ PLCG1+ Layer 1-6 astrocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - NOSTRIN+ SRGN+ Layer 2-5 endothelial cell Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - NOSTRIN+ SRGN+ Layer 2-5 endothelial cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ KCNG3+ Layer 2 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ KCNG3+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LINC00507+ ATP7B+ Layer 2 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ ATP7B+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LINC00507+ GLRA3+ Layer 2 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ GLRA3+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LINC00507+ DSG3+ Layer 2-3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ DSG3+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ CCDC68+ Layer 2-3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ CCDC68+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ PTPN3+ Layer 2-3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ PTPN3+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ RTKN2+ Layer 2-3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ RTKN2+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ CARM1P1+ Layer 3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CARM1P1+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ OTOGL+ Layer 3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ OTOGL+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ ENPEP+ Layer 3 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ ENPEP+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ ASGR2+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ ASGR2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ LINC01107+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ LINC01107+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ LAMA4+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LAMA4+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ LINC01202+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LINC01202+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ LNX2+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LNX2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ RPRM+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ RPRM+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ TNNT2+ Layer 3-5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ TNNT2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ CSN1S1+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ CSN1S1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ NREP-AS1+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ NREP-AS1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ PKD2L1+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PKD2L1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ RNF144A-AS1+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ RNF144A-AS1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - RORB+ MED8+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ MED8+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ FGF10+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ FGF10+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ LINC01116+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ LINC01116+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ RGPD6+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ RGPD6+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ SLC22A18+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SLC22A18+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ VILL+ Layer 5 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ VILL+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ C9orf135-AS1+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ C9orf135-AS1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ CFTR+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ CFTR+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ FILIP1L+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ FILIP1L+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ IFNG-AS1+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ IFNG-AS1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ LPO+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ LPO+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ OR1L8+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ OR1L8+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ SH2D1B+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ SH2D1B+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ SMYD1+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SMYD1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ TNFAIP6+ Layer 5-6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ TNFAIP6+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ FFAR4+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ FFAR4+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ KLK7+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ KLK7+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ PDYN+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PDYN+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ POGK+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ POGK+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - FEZF2+ PROKR2+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PROKR2+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ LINC00343+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ LINC00343+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ SLN+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SLN+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - THEMIS+ SNTG2+ Layer 6 glutamatergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SNTG2+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ BMP2+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ BMP2+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ NMBR+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ NMBR+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ PVRL2+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ PVRL2+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ RAB11FIP1+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ RAB11FIP1+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PAX6+ CHRFAM7A+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ CHRFAM7A+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PAX6+ MIR101-1+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ MIR101-1+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ SST ASIC4+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ SST ASIC4+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ DEFB108B+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ DEFB108B+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ P4HA3+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ P4HA3+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ KLHDC8B+ Layer 1 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ KLHDC8B+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ CDK20+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ CDK20+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ CCNJL+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CCNJL+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ CLIC6+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CLIC6+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ PRRT4+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ PRRT4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ HTR3A+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HTR3A+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ PTGER3+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ PTGER3+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ SCML4+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SCML4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ WNT4+ Layer 1-2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ WNT4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ FAM20A+ Layer 1-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ FAM20A+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ CBLN1+ Layer 1-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CBLN1+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ CHRNA2+ Layer 1-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CHRNA2+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ FNDC1+ Layer 1-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ FNDC1+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ HSPB6+ Layer 1-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HSPB6+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ CD27-AS1+ Layer 1-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CD27-AS1+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ LINC01013+ Layer 1-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ LINC01013+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ PHLDB3+ Layer 1-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ PHLDB3+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ SMOC1+ Layer 1-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SMOC1+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ AARD+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ AARD+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ CA1+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CA1+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ NES+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ NES+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ COL15A1+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ COL15A1+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ NPY+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ NPY+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ SLC7A6OS+ Layer 1-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SLC7A6OS+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PAX6+ FREM2+ Layer 2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ FREM2+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ FRZB+ Layer 2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ FRZB+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ SLC6A16+ Layer 2 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SLC6A16+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ NMU+ Layer 2-3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ NMU+ Layer 2-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ HHIPL1+ Layer 2-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ HHIPL1+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ RPH3AL+ Layer 2-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ RPH3AL+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ BSPRY+ Layer 2-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ BSPRY+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ SOX11+ Layer 2-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SOX11+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ SAMD13+ Layer 3 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ SAMD13+ Layer 3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ ISG20+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ ISG20+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ CDH3+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CDH3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ GGTLC3+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ GGTLC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ OR5AH1P+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ OR5AH1P+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ HS3ST3A1+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HS3ST3A1+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ IGDCC3+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ IGDCC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ TAC3+ Layer 3-5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ TAC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PAX6+ LINC01497+ Layer 3-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ LINC01497+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ UG0898H09+ Layer 3-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ UG0898H09+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - VIP+ ZIM2-AS1+ Layer 3-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ ZIM2-AS1+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ LRIG3+ Layer 5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ LRIG3+ Layer 5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - SST+ RPL35AP11+ Layer 5 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ RPL35AP11+ Layer 5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - LAMP5+ CRABP1+ Layer 5-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CRABP1+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ FAM150B+ Layer 5-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ FAM150B+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Motor Cortex - Cluster - PVALB+ GAPDHP60+ Layer 5-6 GABAergic neuron Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ GAPDHP60+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Harmonizome 3.0

Acute Motor Axonal Neuropathy Gene Set

leukemia, erythroblastic, acute; leukemia, megakaryoblastic, acute; leukemia, monocytic, acute; leukemia, myeloid; leukemia, myeloid, acute; leukemia, myelomonocytic, acute; leukemia, promyelocytic, acute Gene Set

Acute Motor Sensory Axonal Neuropathy Gene Set

motor axonal neuropathy Gene Set

Motor Axonal Neuropathy Gene Set

Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set

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

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

Giant axonal neuropathy, autosomal dominant Gene Set

Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene Set

Giant axonal neuropathy Gene Set

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene Set

Giant Axonal Neuropathy Gene Set

axonal neuropathy Gene Set

sensory axonal neuropathy Gene Set

chronic axonal neuropathy Gene Set

peripheral axonal neuropathy Gene Set

neuromyotonia and axonal neuropathy, autosomal recessive Gene Set

giant axonal neuropathy-1 Gene Set

spinocerebellar ataxia, autosomal recessive with axonal neuropathy Gene Set

?giant axonal neuropathy 2, autosomal dominant Gene Set

Axonal Neuropathy Gene Set

Peripheral Axonal Neuropathy Gene Set

Axonal Sensorimotor Neuropathy Gene Set

Chronic Axonal Neuropathy Gene Set

Giant Axonal Neuropathy Gene Set

Giant Axonal Neuropathy, Autosomal Dominant Gene Set

Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene Set

Sensory Axonal Neuropathy Gene Set

Spinocerebellar ataxia with axonal neuropathy 2 Gene Set

Axonal neuropathy Gene Set

Spinocerebellar ataxia with axonal neuropathy type 3 Gene Set

Spinocerebellar ataxia with axonal neuropathy 2 Gene Set

Spinocerebellar ataxia with axonal neuropathy 1 Gene Set

Giant axonal neuropathy 2 Gene Set

Giant axonal neuropathy 1 Gene Set

Peripheral axonal neuropathy Gene Set

Giant axonal neuropathy Gene Set

Autosomal recessive axonal neuropathy Gene Set

GARS-Associated Axonal Neuropathy Gene Set

leukemia, myelocytic, acute; leukemia, myeloid, acute; leukemias, acute myeloblastic Gene Set

acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set

acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma Gene Set

acute lymphocytic leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set

acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

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

Neuropathy, Distal Hereditary Motor, Type IIA 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

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set

Neuropathy, hereditary motor and sensory, LOM type Gene Set

asymmetric motor neuropathy Gene Set

distal hereditary motor neuropathy Gene Set

motor peripheral neuropathy Gene Set

neuropathy, hereditary motor and sensory Gene Set

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

demyelinating motor neuropathy Gene Set

Hereditary Sensory and Motor Neuropathy Gene Set

neuropathy, motor and sensory, russe type Gene Set

neuropathy, distal hereditary motor, jerash 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

neuropathy, distal hereditary motor, type va Gene Set

hereditary motor and sensory neuropathy, type iic Gene Set

hereditary motor and sensory neuropathy vi Gene Set

neuropathy, distal hereditary motor, type viib Gene Set

leukoencephalopathy with dystonia and motor neuropathy 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

Hereditary Motor And Sensory Neuropathy Gene Set