Name

emg: neuropathic changes Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: neuropathic changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Emg: Neuropathic Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Neuropathic Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

neuropathic Gene Set

From GeneRIF Biological Term Annotations

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

neuropathic arthropathy Gene Set

From HPO Gene-Disease Associations

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

acute episodes of neuropathic symptoms Gene Set

From HPO Gene-Disease Associations

genes associated with the acute episodes of neuropathic symptoms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Central Neuropathic Pain Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Central Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Non-Neuropathic Amyloidosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Non-Neuropathic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Peripheral Neuropathic Pain Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Peripheral Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Acute Episodes Of Neuropathic Symptoms Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Acute Episodes Of Neuropathic Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Neuropathic Pain Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

emg: myotonic runs Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: myotonic runs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

emg: chronic denervation signs Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: chronic denervation signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

emg: myopathic abnormalities Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: myopathic abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

emg abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the emg abnormality 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.

emg: impaired neuromuscular transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: impaired neuromuscular transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

emg: decremental response of compound muscle action potential to repetitive nerve stimulation Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: decremental response of compound muscle action potential to repetitive nerve stimulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Emg: Myopathic Abnormalities Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Myopathic Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg: Decremental Response Of Compound Muscle Action Potential To Repetitive Nerve Stimulation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Decremental Response Of Compound Muscle Action Potential To Repetitive Nerve Stimulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg: Impaired Neuromuscular Transmission Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Impaired Neuromuscular Transmission in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Increased Jitter At Single Fibre Emg Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Increased Jitter At Single Fibre Emg in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg: Chronic Denervation Signs Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Chronic Denervation Signs 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.

Emg: Myotonic Runs Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Myotonic Runs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg: Myotonic Discharges Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Myotonic Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg Positive Sharp Waves Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg Positive Sharp Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Emg: Myokymic Discharges Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Emg: Myokymic Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Body Weight Changes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Body Weight Changes from the curated CTD Gene-Disease Associations dataset.

Body Weight Changes Gene Set

From dbGAP Gene-Trait Associations

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

exercise-mediated changes of insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exercise-mediated changes of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; arterial wall changes Gene Set

From GAD Gene-Disease Associations

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

body composition changes Gene Set

From GAD Gene-Disease Associations

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

postmortem changes Gene Set

From GAD Gene-Disease Associations

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

body weight changes Gene Set

From GAD Gene-Disease Associations

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

changes in the concentration of apo b- and apo a-i-containing lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease changes in the concentration of apo b- and apo a-i-containing lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise-induced changes in insulin Gene Set

From GAD Gene-Disease Associations

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

fluvastatin induced cholesterol changes Gene Set

From GAD Gene-Disease Associations

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

arterial wall changes Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; arterial-wall changes; cholesterol efflux Gene Set

From GAD Gene-Disease Associations

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

cardiac conduction disturbances and degenerative changes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac conduction disturbances and degenerative changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

changesin Gene Set

From GeneRIF Biological Term Annotations

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

changes Gene Set

From GeneRIF Biological Term Annotations

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

apoptotic mitochondrial changes Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic mitochondrial changes biological process from the curated GO Biological Process Annotations dataset.

changes to dna methylation involved in embryo development Gene Set

From GO Biological Process Annotations

genes participating in the changes to dna methylation involved in embryo development biological process from the curated GO Biological Process Annotations dataset.

apoptotic nuclear changes Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic nuclear changes biological process from the curated GO Biological Process Annotations dataset.

patchy changes of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the patchy changes of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

patchy changes of bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy changes of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nodular changes affecting the eyelids Gene Set

From HPO Gene-Disease Associations

genes associated with the nodular changes affecting the eyelids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

personality changes Gene Set

From HPO Gene-Disease Associations

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

mood changes Gene Set

From HPO Gene-Disease Associations

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

hypertrophic nerve changes Gene Set

From HPO Gene-Disease Associations

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

scheuermann-like vertebral changes Gene Set

From HPO Gene-Disease Associations

genes associated with the scheuermann-like vertebral changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Postmortem Changes Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

brachyolmia 4 with mild epiphyseal and metaphyseal changes Gene Set

From OMIM Gene-Disease Associations

genes associated with the brachyolmia 4 with mild epiphyseal and metaphyseal changes phenotype from the curated OMIM Gene-Disease Associations dataset.

parathyroid adenoma with cystic changes Gene Set

From OMIM Gene-Disease Associations

genes associated with the parathyroid adenoma with cystic changes phenotype from the curated OMIM Gene-Disease Associations dataset.

Mental Status Changes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Mental Status Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Other Congenital Malformation Syndromes With Other Skeletal Changes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Other Congenital Malformation Syndromes With Other Skeletal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Peau D'Orange Retinal Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Peau D'Orange Retinal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cognitive Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cognitive Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Body Temperature Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Body Temperature Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hypertrophic Nerve Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Hypertrophic Nerve Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Increased Bone Density With Cystic Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Increased Bone Density With Cystic Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Body Weight Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Body Weight Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Scheuermann-Like Vertebral Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Scheuermann-Like Vertebral Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Modic Type Vertebral Endplate Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Modic Type Vertebral Endplate Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

apoptotic mitochondrial changes Gene Set

From GO Biological Process Annotations 2023

genes participating in the apoptotic mitochondrial changes biological process from the curated GO Biological Process Annotations 2023 dataset.

apoptotic nuclear changes Gene Set

From GO Biological Process Annotations 2023

genes participating in the apoptotic nuclear changes biological process from the curated GO Biological Process Annotations 2023 dataset.

spliceosomal conformational changes to generate catalytic conformation Gene Set

From GO Biological Process Annotations 2023

genes participating in the spliceosomal conformational changes to generate catalytic conformation biological process from the curated GO Biological Process Annotations 2023 dataset.