axonal neuropathy

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Results for "axonal neuropathy": 3 genes, 530 gene sets

Name
CMT2H Gene Charcot-Marie-Tooth disease, axonal, type 2H
CMT2G Gene Charcot-Marie-Tooth disease, axonal, type 2G
CNTN2 Gene contactin 2 (axonal) This gene encodes a member of the contactin family of proteins, part of the immunoglobulin superfamily of cell adhesion molecules. The encoded glycosylphosphatidylinositol (GPI)-anchored neuronal membrane protein plays a role in the proliferation, migration, and axon guidance of neurons of the developing cerebellum. A mutation in this gene may be associated with adult myoclonic epilepsy. [provided by RefSeq, Sep 2016]
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auditory neuropathy, autosomal recessive, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Sciatic Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sciatic Neuropathy from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.
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.
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.
Tomaculous neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tomaculous neuropathy from the curated CTD Gene-Disease Associations dataset.
Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
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.
Neuropathy, hereditary motor and sensory, LOM type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset.
Inherited Peripheral Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inherited Peripheral Neuropathy from the curated CTD Gene-Disease Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.
peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease 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.
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.
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.
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.
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.
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.
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.
neuropathy, hereditary motor and sensory Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy type 1b Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth neuropathy type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetic neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber'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.
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, small fiber Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, small fiber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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 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.
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.
Hereditary Sensory and Motor Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Sensory and Motor Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcoholic Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcoholic Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Median Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Median Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
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.
neuropathy, motor and sensory, russe type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, jerash type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy v Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset.
auditory neuropathy, autosomal dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ie Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type id Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type id phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type if Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type if phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital cataracts, facial dysmorphism, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
agenesis of the corpus callosum with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
neuropathy, hereditary motor and sensory, russe type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant, with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, proximal type Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type va Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, recurrent, with pressure palsies Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, inflammatory demyelinating Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, inflammatory demyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type vii Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy vi Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type viib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type v Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type v phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with dystonia and motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, congenital hypomyelinating Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, congenital hypomyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
auditory neuropathy, autosomal recessive, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal recessive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 Motor And Sensory Neuropathy, Type Iic (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary 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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
Congenital hypomyelination neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hypomyelination neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diabetic neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neuropathy x type 2 diabetes interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuropathy x type 2 diabetes interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic peripheral neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic peripheral neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Paclitaxel-induced neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Taxane-induced peripheral neuropathy in breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Taxane-induced peripheral neuropathy in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
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.

Harmonizome 3.0

CMT2H Gene

CMT2G Gene

CNTN2 Gene

axonal neuropathy Gene Set

Axonal Neuropathy Gene Set

Axonal neuropathy 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

sensory axonal neuropathy Gene Set

chronic axonal neuropathy Gene Set

peripheral axonal neuropathy Gene Set

motor 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

Peripheral Axonal Neuropathy Gene Set

Axonal Sensorimotor Neuropathy Gene Set

Chronic Axonal Neuropathy Gene Set

Giant Axonal Neuropathy Gene Set

Acute Motor Axonal Neuropathy Gene Set

Giant Axonal Neuropathy, Autosomal Dominant Gene Set

Acute Motor Sensory Axonal Neuropathy Gene Set

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

Motor Axonal Neuropathy Gene Set

Sensory Axonal Neuropathy Gene Set

Spinocerebellar ataxia with axonal neuropathy 2 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

Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set

GARS-Associated Axonal Neuropathy Gene Set

Charcot-Marie-Tooth disease, axonal, type 2s Gene Set

Charcot-Marie-Tooth disease, axonal, type 2r Gene Set

Charcot-Marie-Tooth disease, axonal, type 2q Gene Set

axonal growth cone Gene Set

axonal spine Gene Set

axonal growth cone Gene Set

axonal spine Gene Set

Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set

Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set

Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set

axonal Gene Set

mammillothalamic axonal tract development Gene Set

axonal fasciculation Gene Set

axonal growth cone Gene Set

axonal spine Gene Set

axonal degeneration/regeneration Gene Set

axonal loss Gene Set

peripheral axonal atrophy Gene Set

emg: axonal abnormality Gene Set

axonal regeneration Gene Set

peripheral axonal degeneration Gene Set

diffuse axonal swelling Gene Set

clusters of axonal regeneration Gene Set

mixed demyelinating and axonal polyneuropathy Gene Set

axonal dystrophy Gene Set

abnormal axonal transport Gene Set

axonal spheroids Gene Set

charcot-marie-toothe disease, axonal, type 2p Gene Set

charcot-marie-tooth disease, axonal, type 2s Gene Set

charcot-marie-tooth disease, axonal, type 2k Gene Set

charcot-marie-tooth disease, axonal, type 2n Gene Set

charcot-marie-tooth disease, axonal, type 2m Gene Set

charcot-marie-tooth disease, axonal, type 2g Gene Set

charcot-marie-tooth disease, axonal, type 2f Gene Set

charcot-marie-tooth disease, axonal, type 20 Gene Set

?charcot-marie-tooth disease, axonal, type 2q Gene Set

charcot-marie-tooth disease, axonal, with vocal cord paresis Gene Set