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Familial Idiopathic Pulmonary Fibrosis Gene SetFrom 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 Pulmonary Fibrosis Gene SetFrom 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 SetFrom 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 pulmonary fibrosis Gene SetFrom 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 pulmonary fibrosis Gene SetFrom 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 pulmonary fibrosis Gene SetFrom 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 pulmonary fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
idiopathic pulmonary fibrosis Gene SetFrom 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. |
Idiopathic Pulmonary Fibrosis Gene SetFrom 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. |
pulmonary fibrosis, idiopathic Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary fibrosis, idiopathic, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
idiopathic pulmonary fibrosis Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom 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. |
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene SetFrom 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. |
Chronic Idiopathic Pulmonary Fibrosis Gene SetFrom 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 pulmonary fibrosis cell_Lung_Human Gene SetFrom 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 SetFrom 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. |
Idiopathic pulmonary fibrosis disease specific cell type Gene SetFrom 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 Pulmonary Fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Idiopathic pulmonary fibrosis Gene SetFrom 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. |
fibrosis; pulmonary fibrosis; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Idiopathic and/or familial pulmonary arterial hypertension Gene SetFrom 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 Retroperitoneal Fibrosis Gene SetFrom 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. |
Idiopathic Pulmonary Arterial Hypertension Gene SetFrom 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 Hypertension Gene SetFrom 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. |
Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia Gene SetFrom 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. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pulmonary fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
diffuse pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
localized pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung neoplasms; neoplasm of lung ; pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung neoplasms; neoplasm of lung ; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; pigeon breeders disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; pigeon breeders disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chemotherapy-induced pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chemotherapy-induced pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; sarcoidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; scleroderma, systemic; systemic scleroderma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung diseases, interstitial; pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung diseases, interstitial; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the pulmonary fibrosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
pulmonary fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary aterial intimal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary aterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Pulmonary Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
pulmonary fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{pulmonary fibrosis, telomere-related, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Combined Pulmonary Fibrosis And Emphysema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Combined Pulmonary Fibrosis And Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Fibrosis - From Asbestos Exposure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis - From Asbestos Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Aterial Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Aterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Postinflammatory pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Postinflammatory pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diffuse pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Localized pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary fibrosis and/or bone marrow failure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diffuse interstitial pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse interstitial pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary fibrosis and/or bone marrow failure syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
short stature, idiopathic familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Idiopathic Hypercalciuria Gene SetFrom 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 Familial Dystonia Gene SetFrom 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 Non-Familial Dystonia Gene SetFrom 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. |
Familial idiopathic steroid-resistant nephrotic syndrome Gene SetFrom 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. |
Familial idiopathic hypercalciuria Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic hypercalciuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial idiopathic inflammatory myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
cystic fibrosis; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; pulmonary disease, chronic obstructive; pulmonary emphysema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary disease, chronic obstructive; pulmonary emphysema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis, pulmonary; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis, pulmonary; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Pulmonary Veno-Occlusive Disease And/Or Pulmonary Capillary Hemangiomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Veno-Occlusive Disease And/Or Pulmonary Capillary Hemangiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Embolism With Pulmonary Infarction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pulmonary Embolism With Pulmonary Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pulmonary vascular system_CT1_smooth muscle cell of the pulmonary artery Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Pulmonary vascular system_CT1_smooth muscle cell of the pulmonary artery cell type from the HuBMAP ASCT+B dataset. |
Pulmonary vascular system_CT1_fibroblast of pulmonary artery Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Pulmonary vascular system_CT1_fibroblast of pulmonary artery cell type from the HuBMAP ASCT+B dataset. |
Pulmonary vascular system_CT1_fibroblast of pulmonary artery Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Pulmonary vascular system_CT1_fibroblast of pulmonary artery cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Pulmonary vascular system_CT1_smooth muscle cell of the pulmonary artery Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Pulmonary vascular system_CT1_smooth muscle cell of the pulmonary artery cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Pulmonary artery enlargement and chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary artery enlargement and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulmonary artery enlargement in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary artery enlargement in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Familial pulmonary capillary hemangiomatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension, familial primary, 1, with or without hht Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Primary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial pulmonary capillary hemangiomatosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset. |
amyloidosis, familial; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; amyloidosis, familial; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple familial trichoepithelioma and familial cylindromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis, familial; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hemiplegic migraine and benign familial infantile convulsions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Short stature, idiopathic, autosomal Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Hypogonadotropic Hypogonadism from the curated CTD Gene-Disease Associations dataset. |
idiopathic interstitial pneumonia Gene SetFrom 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 juvenile osteoporosis Gene SetFrom 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 generalized epilepsy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Gene SetFrom 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 SetFrom 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. |
Arthritis (juvenile idiopathic) Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Hypersomnolence, Idiopathic Gene SetFrom 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 SetFrom 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 Interstitial Pneumonias Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, idiopathic generalized, susceptibility to 4 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
scoliosis, idiopathic 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
basal ganglia calcification, idiopathic, 5 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pancreatitis, idiopathic} Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Adolescent Idiopathic Scoliosis Gene SetFrom 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 SetFrom 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 SetFrom 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 Nephrotic Syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Scoliosis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Idiopathic Hypercalciuria Gene SetFrom 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. |
Idiopathic Premature Ovarian Failure Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Central Precocious Puberty Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Idiopathic Urethral Stricture Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Copper Toxicosis, Idiopathic Gene SetFrom 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. |
Idiopathic Eosinophilic Myositis Gene SetFrom 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. |
Anterior Uveitis Idiopathic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Idiopathic Myoclonic Epilepsy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) Gene Setproteins participating in the Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) pathway from the Reactome Pathways 2024 dataset. |
Idiopathic generalized epilepsy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 generalized epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Idiopathic nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Idiopathic basal ganglia calcification Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Idiopathic scoliosis Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic environmental intolerance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Systemic juvenile idiopathic arthritis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 inflammatory myopathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
Fibrosis of extraocular muscles, congenital, 3b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cystic fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oral Submucous Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Oral Submucous Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Peritoneal Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peritoneal Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Endomyocardial Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Endomyocardial Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset. |
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cystic Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Fibrosis of Extraocular Muscles, Congenital, 3B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset. |
CYSTIC FIBROSIS, MODIFIER OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CYSTIC FIBROSIS, MODIFIER OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Cystic Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
cystic fibrosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cystic fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cystic fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
oral submucous fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endomyocardial fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
preretinal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cholestasis, intrahepatic; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; ileus; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; lung diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes mellitus, type 1; hyperglycemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus, type 1; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; candida Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; candida in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colonic diseases; cystic fibrosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic diseases; cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; lung diseases; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic iron and fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic iron and fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis lung disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis lung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; rhinitis; sinusitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; ileus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; disease susceptibility; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease susceptibility; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; retroperitoneal fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; retroperitoneal fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; intussusception Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; intussusception in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; fibrosis; mouth neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; fibrosis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung allograft fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung allograft fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; disease models, animal; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease models, animal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cystic fibrosis; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; fibrosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; urogenital abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; protein-energy malnutrition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital fibrosis of the extraocular muscles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; maxillary sinusitis; sinusitis, maxillary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes mellitus; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis b, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis b, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
clonorchiasis; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease clonorchiasis; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; steatorrhea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; lung diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral submucous fibrosis; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
burkholderia infections; cystic fibrosis; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease burkholderia infections; cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; neoplasms; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; dental caries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dental caries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; paranasal sinus diseases; sinus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; paranasal sinus diseases; sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aspergillosis; cystic fibrosis; lung diseases, fungal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aspergillosis; cystic fibrosis; lung diseases, fungal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; gastrointestinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hcv-induced liver fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hcv-induced liver fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; growth disorders; nutrition disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; growth disorders; nutrition disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cystic fibrosis; ileus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; p. aeruginosa infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; p. aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; fibrosis; mammary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; fibrosis; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; lung diseases, interstitial; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases, interstitial; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral cancer; oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral cancer; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fibrosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Cystic fibrosis severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hepatitis C induced liver fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
cystic fibrosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
tubulointerstitial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pancreatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pancreatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital hepatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
myocardial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the myocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arterial intimal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the arterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
portal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the portal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retroperitoneal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the retroperitoneal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
perifollicular fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the perifollicular fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
endocardial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the endocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
periportal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the periportal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Oral Submucous Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Oral Submucous Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cystic Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Cystic Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Retroperitoneal Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Retroperitoneal Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cystic fibrosis transmembrane conductance regulator Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cystic fibrosis transmembrane conductance regulator protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
retinal fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cardiac interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cardiac fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
perivascular fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
urinary bladder fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal glomerulus fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle endomysial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skin fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skin fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cystic fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the cystic fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3b Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3b phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3a Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3a phenotype from the curated OMIM Gene-Disease Associations dataset. |
{cystic fibrosis lung disease, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {cystic fibrosis lung disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{meconium ileus in cystic fibrosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {meconium ileus in cystic fibrosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fibrosis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
cystic fibrosis Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease cystic fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis, Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oral Submucous Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oral Submucous Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Fibrosis, Congenital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peritoneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peritoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Interstitial Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Interstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Fibrosis And Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis And Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Pleura Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pleura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nephrogenic Systemic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nephrogenic Systemic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Classical Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Classical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis In Children Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis Related Diabetes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Related Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis With Meconium Ileus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis With Meconium Ileus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver Disease Associated With Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver Disease Associated With Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sweat Chloride Elevation Without Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sweat Chloride Elevation Without Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Urinary Bladder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Urinary Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ovarian Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Fibrosis Of The Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Fibrosis Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oesophageal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Corpus Cavernosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Corpus Cavernosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis, Neurodegeneration, And Cerebral Angiomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Neurodegeneration, And Cerebral Angiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis Modifier 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Modifier 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prostatic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Portal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Portal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tubulointerstitial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubulointerstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intestinal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Endomyocardial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endomyocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Periportal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periportal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skeletal Muscle Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Of Mesentery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Mesentery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Myocardial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Perifollicular Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perifollicular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
pancreas fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cardiac fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cardiac interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
liver fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the liver fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle endomysial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skin fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skin fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
urinary bladder fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
retina fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerulus fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
perivascular fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
spleen fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
trachea fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the trachea fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intestinal fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
epididymis fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
uterus fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Lung fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Lung fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
HIPK2 in kidney fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the HIPK2 in kidney fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
Nitric oxide metabolism in cystic fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Nitric oxide metabolism in cystic fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
Defective CFTR causes cystic fibrosis Gene Setproteins participating in the Defective CFTR causes cystic fibrosis pathway from the Reactome Pathways 2024 dataset. |
Cystic fibrosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cystic fibrosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital fibrosis of the extraocular muscles from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Cystic fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Oral submucous fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Preretinal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endomyocardial fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 3A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cystic fibrosis disease specific cell type Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cystic fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periportal fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periportal fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cystic fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cystic fibrosis-gastritis-megaloblastic anemia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis-gastritis-megaloblastic anemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatorenocardiac degenerative fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatorenocardiac degenerative fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Meconium ileus in cystic fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meconium ileus in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis and steatohepatitis severity (MRI cT1 measure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis and steatohepatitis severity (MRI cT1 measure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung disease severity in cystic fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung disease severity in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis severity in HIV/hepatitis C co-infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis severity in HIV/hepatitis C co-infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis in pediatric non-alcoholic fatty acid liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in pediatric non-alcoholic fatty acid liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis (total hepatic collagen content) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis (total hepatic collagen content) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cystic fibrosis-related diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis-related diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hepatitis C induced liver fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis in non-alcoholic fatty liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cystic fibrosis severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary hypertension, primary, fenfluramine-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, fenfluramine-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary alveolar microlithiasis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary alveolar microlithiasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alveolar capillary dysplasia with misalignment of pulmonary veins Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary Surfactants Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Pulmonary Surfactants from the curated CTD Gene-Chemical Interactions dataset. |
Pulmonary Embolism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Embolism from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Pulmonary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Pulmonary from the curated CTD Gene-Disease Associations dataset. |
PULMONARY FUNCTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY FUNCTION from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Alveolar Microlithiasis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Alveolar Microlithiasis from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Emphysema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Emphysema from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Eosinophilia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Eosinophilia from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Veno-Occlusive Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset. |
Anophthalmia with pulmonary hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anophthalmia with pulmonary hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Edema from the curated CTD Gene-Disease Associations dataset. |
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset. |
Plasma Cell Granuloma, Pulmonary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Plasma Cell Granuloma, Pulmonary from the curated CTD Gene-Disease Associations dataset. |
Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Tuberculosis, Pulmonary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tuberculosis, Pulmonary from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
chronic pulmonary heart disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic pulmonary heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary pulmonary hypertension from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
pulmonary emphysema Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pulmonary emphysema in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
chronic obstructive pulmonary disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease chronic obstructive pulmonary disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
pulmonary edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary embolism Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary embolism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic pulmonary heart disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic pulmonary heart disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary eosinophilia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary eosinophilia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary alveolar proteinosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary alveolar proteinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary plasma cell granuloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary plasma cell granuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary sarcoidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary sarcoidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary venoocclusive disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary venoocclusive disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary valve stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary sclerosing hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary sclerosing hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary alveolar microlithiasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary alveolar microlithiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary immaturity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary immaturity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary neuroendocrine tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary neuroendocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acute pulmonary heart disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute pulmonary heart disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary systemic sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary systemic sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary blastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary blastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary valve insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic obstructive pulmonary disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic obstructive pulmonary disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary aspergilloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary aspergilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary large cell neuroendocrine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary large cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hantavirus pulmonary syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hantavirus pulmonary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary artery leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary artery leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary emphysema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary emphysema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
H3K4me3_fibroblast of pulmonary artery_hg19_1 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of pulmonary artery_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
H3K4me3_fibroblast of pulmonary artery_hg19_2 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of pulmonary artery_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
CTCF_fibroblast of pulmonary artery_hg19_2 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of pulmonary artery_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
CTCF_fibroblast of pulmonary artery_hg19_1 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of pulmonary artery_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cicatrization; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cicatrization; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary sarcoidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
occupational diseases; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease occupational diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis, pulmonary; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis, pulmonary; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asbestos-associated pulmonary disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asbestos-associated pulmonary disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary function; nitric oxide; pseudomonas aeruginosa infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary function; nitric oxide; pseudomonas aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
connective tissue diseases; hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
copd ; chronic obstructive pulmonary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease copd ; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial hyperreactivity; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial hyperreactivity; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial diseases; tracheal stenosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial diseases; tracheal stenosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aids-related opportunistic infections; tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aids-related opportunistic infections; tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis; sarcoidosis, pulmonary; uveitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis; sarcoidosis, pulmonary; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; hypertension; hypertension, pulmonary; tricuspid valve insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; hypertension; hypertension, pulmonary; tricuspid valve insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary emphysema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis; sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, deep vein; pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism, venous; c-reactive protein; pulmonary embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism, venous; c-reactive protein; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tuberculosis, multidrug-resistant; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tuberculosis, multidrug-resistant; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary disease, mycobacterium malmoense Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary disease, mycobacterium malmoense in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
emphysema; pulmonary disease, chronic obstructive; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease emphysema; pulmonary disease, chronic obstructive; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; pulmonary embolism; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv infections; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary function Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenomatosis, pulmonary; hyperplasia; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenomatosis, pulmonary; hyperplasia; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altitude sickness; chromosome deletion; pulmonary edema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altitude sickness; chromosome deletion; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; dermatitis, atopic; chronic obstructive pulmonary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tuberculosis, meningeal; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tuberculosis, meningeal; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary edema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; kidney failure, acute; postoperative complications; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; kidney failure, acute; postoperative complications; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
erythema nodosum; sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease erythema nodosum; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenomatosis, pulmonary; lung neoplasms; neoplasm invasiveness; neoplasm of lung ; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenomatosis, pulmonary; lung neoplasms; neoplasm invasiveness; neoplasm of lung ; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypercalcemia; sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypercalcemia; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary function measures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary function measures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
raeder-harbitz syndrome; takayasu arteritis; tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease raeder-harbitz syndrome; takayasu arteritis; tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
emphysema; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease emphysema; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, portal; hypertension, pulmonary; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, portal; hypertension, pulmonary; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
phlebitis; pulmonary embolism; varicose veins; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease phlebitis; pulmonary embolism; varicose veins; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anthracosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anthracosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug-induced liver injury; liver diseases; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug-induced liver injury; liver diseases; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthenia; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthenia; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary tuberculosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus, systemic; sjogren's syndrome; systemic lupus erythematosus; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; sjogren's syndrome; systemic lupus erythematosus; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postoperative complications; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postoperative complications; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphadenitis; tuberculosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphadenitis; tuberculosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obstructive pulmonary disease and disseminated bronchiectasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obstructive pulmonary disease and disseminated bronchiectasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
down syndrome; heart defects, congenital; hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary function traits (other) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary function traits (other) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tropical pulmonary eosinophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tropical pulmonary eosinophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altitude sickness; pulmonary edema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altitude sickness; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; hypertension, pulmonary; necrosis; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; hypertension, pulmonary; necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; chronic obstructive pulmonary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-altitude pulmonary edema. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-altitude pulmonary edema. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart anomalies, congenital; pulmonary hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; kidney diseases; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; kidney diseases; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease ; asthma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease ; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis, pulmonary; splenomegaly Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis, pulmonary; splenomegaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sarcoidosis, pulmonary; uveitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sarcoidosis, pulmonary; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cough; dyspnea; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cough; dyspnea; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug-induced liver injury; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug-induced liver injury; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart septal defects, ventricular; hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease/copd; emphysema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leprosy; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leprosy; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term pulmonary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
COPD - Chronic obstructive pulmonary disease_Lung Tissue_GSE1650 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Lung Tissue_GSE1650 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Primary pulmonary hypoplasia_Lung Tissue_GSE1363 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Primary pulmonary hypoplasia_Lung Tissue_GSE1363 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
COPD - Chronic obstructive pulmonary disease_Bronchial epithelium_GSE3320 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Bronchial epithelium_GSE3320 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
pulmonary valve morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
pulmonary vein morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary vein morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
pulmonary valve formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary valve formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
pulmonary artery morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary artery morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
pulmonary artery endothelial tube morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary artery endothelial tube morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
pulmonary myocardium development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pulmonary myocardium development biological process from the curated GO Biological Process Annotations 2015 dataset. |
Pulmonary function Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Pulmonary function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma or chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Body mass in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease (severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Pulmonary function decline Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Pulmonary function decline phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Pulmonary function (interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Pulmonary function (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease (moderate to severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic obstructive pulmonary disease-related biomarkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease-related biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
pulmonary embolism Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease pulmonary embolism in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
pulmonary systemic sclerosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease pulmonary systemic sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
pulmonary emphysema Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease pulmonary emphysema in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
chronic obstructive pulmonary disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
pulmonary embolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the pulmonary embolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
decreased pulmonary function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the decreased pulmonary function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chronic obstructive pulmonary disease Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
pulmonary embolism Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary embolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary arterial medial hypertrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary arterial medial hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic obstructive pulmonary disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anomalous pulmonary venous return Gene SetFrom HPO Gene-Disease Associations genes associated with the anomalous pulmonary venous return phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral pulmonary artery stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary infiltrates Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary infiltrates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery dilatation Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral primary pulmonary dysgenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral primary pulmonary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent pulmonary artery Gene SetFrom HPO Gene-Disease Associations genes associated with the absent pulmonary artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary capillary hemangiomatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary capillary hemangiomatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bicuspid pulmonary valve Gene SetFrom HPO Gene-Disease Associations genes associated with the bicuspid pulmonary valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary valve defects Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary valve defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery vasoconstriction Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery vasoconstriction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplastic pulmonary veins Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic pulmonary veins phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased pulmonary vascular resistance Gene SetFrom HPO Gene-Disease Associations genes associated with the increased pulmonary vascular resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery sling Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery sling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary insufficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive pulmonary function impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive pulmonary function impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral pulmonary vessel aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral pulmonary vessel aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary veins Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary veins phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary lymphangiectasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary lymphangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interstitial pulmonary disease Gene SetFrom HPO Gene-Disease Associations genes associated with the interstitial pulmonary disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary venoocclusive disease Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary venoocclusive disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased pulmonary function Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased pulmonary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
agenesis of pulmonary vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the agenesis of pulmonary vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated pulmonary artery pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated pulmonary artery pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
total anomalous pulmonary venous return Gene SetFrom HPO Gene-Disease Associations genes associated with the total anomalous pulmonary venous return phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Pulmonary Embolism Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Embolism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Pulmonary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Pulmonary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Disease, Chronic Obstructive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Aspergillosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Aspergillosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Valve Stenosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hantavirus Pulmonary Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hantavirus Pulmonary Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Emphysema Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Emphysema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Blastoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Blastoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Eosinophilia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Eosinophilia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sarcoidosis, Pulmonary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sarcoidosis, Pulmonary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Alveolar Proteinosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Alveolar Proteinosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Edema Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Edema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Heart Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Heart Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Tuberculosis, Pulmonary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Tuberculosis, Pulmonary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
increased pulmonary ventilation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary ventilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary respiratory rate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
total anomalous pulmonary venous connection Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the total anomalous pulmonary venous connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
overexpanded pulmonary alveoli Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the overexpanded pulmonary alveoli phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary vascular resistance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pulmonary endothelial cell surface Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary endothelial cell surface phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased number of pulmonary neuroendocrine bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary valve stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pulmonary vascular resistance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aorta pulmonary collateral arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aorta pulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pulmonary respiratory rate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary artery stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary alveoli Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary alveoli phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary circulation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary circulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary valve cusp morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary valve cusp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
patent pulmonary valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the patent pulmonary valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary interalveolar septum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary interalveolar septum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary neuroendocrine bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary valve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary valve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
right pulmonary isomerism Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the right pulmonary isomerism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hyperemia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hyperemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
total anomalous pulmonary venous connection, intracardiac Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the total anomalous pulmonary venous connection, intracardiac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary valve regurgitation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary valve regurgitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal solitary pulmonary neuroendocrine cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal solitary pulmonary neuroendocrine cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary acinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary acinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary trunk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary trunk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary collagen fibril morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar sac morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar sac morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary artery Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
anomalous pulmonary venous connection Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the anomalous pulmonary venous connection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary neuroendocrine body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary neuroendocrine body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bicuspid pulmonary valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bicuspid pulmonary valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary vein Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary vein phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pulmonary trunk Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pulmonary trunk phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolus epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolus epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
supravalvar pulmonary trunk stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the supravalvar pulmonary trunk stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary arteriovenous malformation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary edema Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary interalveolar septum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary interalveolar septum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar parenchyma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar parenchyma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pulmonary vascular resistance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar proteinosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar proteinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary elastic fiber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary elastic fiber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary valve atresia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged pulmonary valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged pulmonary valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary gas exchange Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary gas exchange phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary trunk hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary trunk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar edema Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolus epithelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolus epithelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pulmonary alveolar ducts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pulmonary alveolar ducts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary ventilation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary ventilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pulmonary trunk Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pulmonary trunk phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent solitary pulmonary neuroendocrine cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent solitary pulmonary neuroendocrine cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolus wall morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolus wall morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick pulmonary valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick pulmonary valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
calcified pulmonary alveolus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the calcified pulmonary alveolus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pulmonary respiratory rate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased number of pulmonary neuroendocrine bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased solitary pulmonary neuroendocrine cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary vascular congestion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary vascular congestion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
left pulmonary isomerism Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the left pulmonary isomerism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pulmonary artery pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary artery pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased solitary pulmonary neuroendocrine cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pulmonary artery Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pulmonary artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pulmonary ventilation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary ventilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary epithelial necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary epithelial necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary artery hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary endothelial cell surface Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary endothelial cell surface phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{pulmonary disease, chronic obstructive, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary disease, chronic obstructive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary alveolar microlithiasis Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary alveolar microlithiasis phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary function} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary function} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
alveolar capillary dysplasia with misalignment of pulmonary veins Gene SetFrom OMIM Gene-Disease Associations genes associated with the alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary venoocclusive disease 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary venoocclusive disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary venoocclusive disease 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary venoocclusive disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary disease, chronic obstructive, severe early-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary hypertension, neonatal, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, neonatal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
total anomalous pulmonary venous return Gene SetFrom OMIM Gene-Disease Associations genes associated with the total anomalous pulmonary venous return phenotype from the curated OMIM Gene-Disease Associations dataset. |