Copper Toxicosis, Idiopathic

Clear Filter

Results for "Copper Toxicosis, Idiopathic": 415 gene sets

Name
Copper Toxicosis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Copper Toxicosis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
toxicosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term toxicosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
copper sulfate-500 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-500 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
copper sulfate-438 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-438 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
copper sulfate-459 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-459 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
copper sulfate-575 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-575 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
copper bis(3,5-diisopropylsalicylate) Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper bis(3,5-diisopropylsalicylate) from the curated CTD Gene-Chemical Interactions dataset.
copper protoporphyrin IX Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper protoporphyrin IX from the curated CTD Gene-Chemical Interactions dataset.
Copper Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper from the curated CTD Gene-Chemical Interactions dataset.
bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) from the curated CTD Gene-Chemical Interactions dataset.
copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex from the curated CTD Gene-Chemical Interactions dataset.
(4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) from the curated CTD Gene-Chemical Interactions dataset.
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) from the curated CTD Gene-Chemical Interactions dataset.
Copper Sulfate Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper Sulfate from the curated CTD Gene-Chemical Interactions dataset.
copper (N-2-hydroxyacetophenone)glycinate Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (N-2-hydroxyacetophenone)glycinate from the curated CTD Gene-Chemical Interactions dataset.
copper histidine Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper histidine from the curated CTD Gene-Chemical Interactions dataset.
copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) from the curated CTD Gene-Chemical Interactions dataset.
copper Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term copper in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cellular copper ion homeostasis Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of copper ion transmembrane transport Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion transport Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion import Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion homeostasis Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset.
detoxification of copper ion Gene Set From GO Biological Process Annotations 2015 genes participating in the detoxification of copper ion biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion export Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2015 dataset.
response to copper ion Gene Set From GO Biological Process Annotations 2015 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion import into cell Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion import into cell biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to copper ion Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to copper ion starvation Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2015 dataset.
intracellular copper ion transport Gene Set From GO Biological Process Annotations 2015 genes participating in the intracellular copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset.
plasma membrane copper ion transport Gene Set From GO Biological Process Annotations 2015 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion transmembrane transport Gene Set From GO Biological Process Annotations 2015 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset.
copper ion transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper ion binding Gene Set From GO Molecular Function Annotations 2015 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper uptake transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the copper uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
heme-copper terminal oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the heme-copper terminal oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper chaperone activity Gene Set From GO Molecular Function Annotations 2015 genes performing the copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper-transporting atpase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the copper-transporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper-dependent protein binding Gene Set From GO Molecular Function Annotations 2015 genes performing the copper-dependent protein binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
superoxide dismutase copper chaperone activity Gene Set From GO Molecular Function Annotations 2015 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
copper-exporting atpase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the copper-exporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
abnormality of copper homeostasis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
Copper Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Copper metabolite from the curated HMDB Metabolites of Enzymes dataset.
abnormality of copper homeostasis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
high nonceruloplasmin-bound serum copper Gene Set From HPO Gene-Disease Associations genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Copper amine oxidase, N2/N3-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2/N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase copper chaperone Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase copper chaperone protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper centre Cu(A) Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper centre Cu(A) protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aromatic amino acid hydroxylase, iron/copper binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aromatic amino acid hydroxylase, iron/copper binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper homeostasis protein CutC Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis protein CutC protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Uncharacterised domain, di-copper centre Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised domain, di-copper centre protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper chaperone SCO1/SenC Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper chaperone SCO1/SenC protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper type II, ascorbate-dependent monooxygenase-like, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Tyrosinase copper-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosinase copper-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ctr copper transporter Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ctr copper transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Superoxide dismutase, copper/zinc, binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Superoxide dismutase, copper/zinc binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Heavy metal-associated domain, copper ion-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy metal-associated domain, copper ion-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Amyloidogenic glycoprotein, copper-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Amyloidogenic glycoprotein, copper-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Periplasmic copper-binding protein NosD, beta helix domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Periplasmic copper-binding protein NosD, beta helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N2-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper type II, ascorbate-dependent monooxygenase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N3-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multicopper oxidase, copper-binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multi-copper polyphenol oxidoreductase, laccase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multi-copper polyphenol oxidoreductase, laccase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper homeostasis CutC domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis CutC domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit I, copper-binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit I, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
decreased circulating copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal liver copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased intestine copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal circulating copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal intestine copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal copper homeostasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brain copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased liver copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased brain copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased kidney copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased circulating copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal kidney copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brain copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Copper-Overload Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Copper-Overload Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Copper Homeostasis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Copper Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
High Nonceruloplasmin-Bound Serum Copper Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Nonceruloplasmin-Bound Serum Copper in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Copper Accumulation In Liver Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Copper Accumulation In Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Urinary Copper Concentration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Urinary Copper Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
copper ion transport Gene Set From GO Biological Process Annotations 2023 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset.
protein maturation by copper ion transfer Gene Set From GO Biological Process Annotations 2023 genes participating in the protein maturation by copper ion transfer biological process from the curated GO Biological Process Annotations 2023 dataset.
copper ion import Gene Set From GO Biological Process Annotations 2023 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2023 dataset.
plasma membrane copper ion transport Gene Set From GO Biological Process Annotations 2023 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset.
intracellular copper ion homeostasis Gene Set From GO Biological Process Annotations 2023 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset.
response to copper ion Gene Set From GO Biological Process Annotations 2023 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to copper ion Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to copper ion starvation Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset.
copper ion homeostasis Gene Set From GO Biological Process Annotations 2023 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset.
copper ion export Gene Set From GO Biological Process Annotations 2023 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2023 dataset.
copper ion transmembrane transport Gene Set From GO Biological Process Annotations 2023 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset.
response to copper ion starvation Gene Set From GO Biological Process Annotations 2023 genes participating in the response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset.
copper ion binding Gene Set From GO Molecular Function Annotations 2023 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
copper ion transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
P-type divalent copper transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
superoxide dismutase copper chaperone activity Gene Set From GO Molecular Function Annotations 2023 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
P-type monovalent copper transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
decreased brain copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal copper homeostasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased liver copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal liver copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased brain copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased liver copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased circulating copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased circulating copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased kidney copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased intestine copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased brainstem copper level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brainstem copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Copper homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the Copper homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Copper metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Copper metabolism pathway from the WikiPathways Pathways 2024 dataset.
copper ion transport Gene Set From GO Biological Process Annotations 2025 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset.
copper ion import Gene Set From GO Biological Process Annotations 2025 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2025 dataset.
plasma membrane copper ion transport Gene Set From GO Biological Process Annotations 2025 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset.
intracellular copper ion homeostasis Gene Set From GO Biological Process Annotations 2025 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset.
response to copper ion Gene Set From GO Biological Process Annotations 2025 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to copper ion Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset.
copper ion homeostasis Gene Set From GO Biological Process Annotations 2025 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset.
copper ion export Gene Set From GO Biological Process Annotations 2025 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2025 dataset.
copper ion transmembrane transport Gene Set From GO Biological Process Annotations 2025 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset.
copper ion binding Gene Set From GO Molecular Function Annotations 2025 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
copper ion transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
P-type divalent copper transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
superoxide dismutase copper chaperone activity Gene Set From GO Molecular Function Annotations 2025 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
P-type monovalent copper transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Copper deficiency myelopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Copper deficiency myelopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Copper ion transmembrane transporter complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Copper ion transmembrane transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Superoxide dismutase copper chaperone complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Superoxide dismutase copper chaperone complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Copper levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Copper levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
COPPER CHLORIDE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the COPPER CHLORIDE drug from theDGIdb Drug Targets 2026 dataset.
Short stature, idiopathic, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutropenia, nonimmune chronic idiopathic, of adults Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Basal ganglia calcification, idiopathic, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia calcification, idiopathic, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic hypercalcemia of infancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic hypercalcemia of infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, idiopathic, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic fibrosing alveolitis, chronic form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic fibrosing alveolitis, chronic form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.
Idiopathic dilation cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic dilation cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Purpura, Thrombocytopenic, Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura, Thrombocytopenic, Idiopathic from the curated CTD Gene-Disease Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrotic syndrome, idiopathic, steroid-resistant from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic basal ganglia calcification 1 from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Nonimmune Chronic Idiopathic, Adult Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Nonimmune Chronic Idiopathic, Adult from the curated CTD Gene-Disease Associations dataset.
Jaundice, Chronic Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Chronic Idiopathic from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Hypogonadotropic Hypogonadism from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic interstitial pneumonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic cd4-positive t-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic cd4-positive t-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
systemic juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease systemic juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriage. Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic thrombotic thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic thrombotic thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic premature ovarian failure Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriages Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic infertility Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic deep venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic deep venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonfamilial idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nonfamilial idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic short stature Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic atrial fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic atrial fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic environmental intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic environmental intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypersomnolence, idiopathic; narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypersomnolence, idiopathic; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, idiopathic dilated Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, idiopathic dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic idiopathic neutropenia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic idiopathic neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis (juvenile idiopathic) Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis (juvenile idiopathic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic chronic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic chronic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic orthostatic intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic orthostatic intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent or chronic idiopathic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic torsion dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, idiopathic thrombocytopenic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, idiopathic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood idiopathic thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema Gene Set From GAD Gene-Disease Associations genes associated with the disease graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic; werlhof's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic; werlhof's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic azoospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic azoospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy, idiopathic inflammatory Gene Set From GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter infections; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter infections; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term idiopathic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Nephropathy (idiopathic membranous) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Nephropathy (idiopathic membranous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
idiopathic interstitial pneumonia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic interstitial pneumonia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypersomnolence, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Purpura, Thrombocytopenic, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Thrombocytopenic, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Interstitial Pneumonias phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hyperostosis, Diffuse Idiopathic Skeletal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperostosis, Diffuse Idiopathic Skeletal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, nonimmune chronic idiopathic, of adults Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary fibrosis, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypereosinophilic syndrome, idiopathic, resistant to imatinib Gene Set From OMIM Gene-Disease Associations genes associated with the hypereosinophilic syndrome, idiopathic, resistant to imatinib phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary fibrosis, idiopathic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
hydrocephalus with congenital idiopathic intestinal pseudoobstruction Gene Set From OMIM Gene-Disease Associations genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{pancreatitis, idiopathic} Gene Set From OMIM Gene-Disease Associations genes associated with the {pancreatitis, idiopathic} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Achalasia Of Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Achalasia Of Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Inflammatory Myopathies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Inflammatory Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Bronchiectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Arterial Calcification Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Arterial Calcification Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypereosinophilic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypereosinophilic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Crescentic Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Crescentic Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Urticaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Normal Pressure Hydrocephalus (Inph) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Normal Pressure Hydrocephalus (Inph) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Premature Ovarian Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Premature Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Membranous Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pneumonia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pneumonia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trigeminal Neuralgia, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trigeminal Neuralgia, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypoparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Chronic Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Focal Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Focal Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Torsion Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Torsion Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Central Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Interstitial Pneumonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
(Idiopathic) Normal Pressure Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease (Idiopathic) Normal Pressure Hydrocephalus 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.
Idiopathic Transverse Myelitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Transverse Myelitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile And Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile And Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Polypoidal Choroidal Vasculopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Polypoidal Choroidal Vasculopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Urethral Stricture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Urethral Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
T-Lymphocytopenia, Idiopathic Cd4-Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease T-Lymphocytopenia, Idiopathic Cd4-Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Myositis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Myositis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Retroperitoneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Retroperitoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Uveitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Uveitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercatabolic Hypoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercatabolic Hypoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnolence, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia (Itp) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia (Itp) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Gynecomastia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Gynecomastia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Juxtafoveal Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Juxtafoveal Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Granulomatous Mastitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Granulomatous Mastitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Growth Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymyositis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymyositis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Basal Ganglia Calcification 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Basal Ganglia Calcification 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Atrophoderma Of Pasini And Pierini Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Atrophoderma Of Pasini And Pierini in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Idiopathic Intestinal Pseudoobstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Idiopathic Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature, Idiopathic, Autosomal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Extrahepatic Biliary Atresia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypopituitarism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypopituitarism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Cirrhotic Portal Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Cirrhotic Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Diabetes (Mellitus) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Diabetes (Mellitus) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extended Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extended Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Recurrent Pericarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Acute Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Acute Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cd4 Lymphocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cd4 Lymphocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Anaphylaxis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Anaphylaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Angioedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cardiac Hypertrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cardiac Hypertrophy 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.
Psoriatic Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psoriatic Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Guttate Hypomelanosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Guttate Hypomelanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Multicentric Osteolyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Multicentric Osteolyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypertrophic Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypertrophic Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hyperprolactinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hyperprolactinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Autoimmune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Autoimmune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parkinsonism Or Parkinson'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parkinsonism Or Parkinson'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Precocious Puberty 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.
Idiopathic Membranous Glomerulopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic Hirsutism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Idiopathic Hirsutism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chronic Idiopathic Constipation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Idiopathic Constipation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic pulmonary fibrosis cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) pathway from the Reactome Pathways 2024 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic scoliosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic scoliosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 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.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic CD4-positive T-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic CD4-positive T-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic pulmonary fibrosis disease specific cell type Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Idiopathic pulmonary fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic steroid-resistant nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic and/or familial pulmonary arterial hypertension Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic and/or familial pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic Pulmonary Fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic basal ganglia calcification Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic basal ganglia calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic hypereosinophilic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic hypereosinophilic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic camptocormia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic camptocormia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic CD4 lymphocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic CD4 lymphocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonimmune chronic idiopathic neutropenia of adults Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonimmune chronic idiopathic neutropenia of adults phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic hypercalciuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic hypercalciuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic scoliosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic environmental intolerance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic environmental intolerance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic inflammatory myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Systemic juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic osteonecrosis of the femoral head Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic downbeat nystagmus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic downbeat nystagmus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic inflammatory myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic membranous nephropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic membranous nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic intracranial hypertension Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic intracranial hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (oligoarticular juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (oligoarticular juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Copper Toxicosis, Idiopathic Gene Set

toxicosis Gene Set

copper sulfate-500 Gene Set

copper sulfate-438 Gene Set

copper sulfate-459 Gene Set

copper sulfate-575 Gene Set

copper bis(3,5-diisopropylsalicylate) Gene Set

copper protoporphyrin IX Gene Set

Copper Gene Set

bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) Gene Set

copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex Gene Set

(4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) Gene Set

(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) Gene Set

Copper Sulfate Gene Set

copper (N-2-hydroxyacetophenone)glycinate Gene Set

copper histidine Gene Set

copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) Gene Set

copper Gene Set

cellular copper ion homeostasis Gene Set

regulation of copper ion transmembrane transport Gene Set

copper ion transport Gene Set

copper ion import Gene Set

copper ion homeostasis Gene Set

detoxification of copper ion Gene Set

copper ion export Gene Set

response to copper ion Gene Set

copper ion import into cell Gene Set

cellular response to copper ion Gene Set

cellular response to copper ion starvation Gene Set

intracellular copper ion transport Gene Set

plasma membrane copper ion transport Gene Set

copper ion transmembrane transport Gene Set

copper ion transmembrane transporter activity Gene Set

copper ion binding Gene Set

copper uptake transmembrane transporter activity Gene Set

heme-copper terminal oxidase activity Gene Set

copper chaperone activity Gene Set

copper-transporting atpase activity Gene Set

copper-dependent protein binding Gene Set

superoxide dismutase copper chaperone activity Gene Set

copper-exporting atpase activity Gene Set

abnormality of copper homeostasis Gene Set

Copper Gene Set

abnormality of copper homeostasis Gene Set

high nonceruloplasmin-bound serum copper Gene Set

Copper amine oxidase, N2/N3-terminal Gene Set

Cytochrome c oxidase copper chaperone Gene Set

Copper centre Cu(A) Gene Set

Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site Gene Set

Aromatic amino acid hydroxylase, iron/copper binding site Gene Set

Copper homeostasis protein CutC Gene Set

Uncharacterised domain, di-copper centre Gene Set

Copper chaperone SCO1/SenC Gene Set

Copper type II, ascorbate-dependent monooxygenase-like, C-terminal Gene Set

Copper amine oxidase, N-terminal Gene Set

Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site Gene Set

Tyrosinase copper-binding domain Gene Set

Ctr copper transporter Gene Set

Superoxide dismutase, copper/zinc, binding site Gene Set

Superoxide dismutase, copper/zinc binding domain Gene Set

Heavy metal-associated domain, copper ion-binding Gene Set

Amyloidogenic glycoprotein, copper-binding Gene Set

Copper amine oxidase Gene Set

Periplasmic copper-binding protein NosD, beta helix domain Gene Set

Copper amine oxidase, N2-terminal Gene Set

Copper type II, ascorbate-dependent monooxygenase, N-terminal Gene Set

Copper amine oxidase, C-terminal Gene Set

Copper amine oxidase, N3-terminal Gene Set

Multicopper oxidase, copper-binding site Gene Set

Multi-copper polyphenol oxidoreductase, laccase Gene Set

Copper homeostasis CutC domain Gene Set

Cytochrome c oxidase, subunit I, copper-binding site Gene Set

decreased circulating copper level Gene Set

abnormal liver copper level Gene Set

decreased liver copper level Gene Set

increased intestine copper level Gene Set

abnormal circulating copper level Gene Set

abnormal intestine copper level Gene Set

abnormal copper homeostasis Gene Set