Name

peripheral pulmonary vessel aplasia Gene Set

From 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.

arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral arterial disease; peripheral arterial diseases Gene Set

From GAD Gene-Disease Associations

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

constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral pulmonary artery stenosis Gene Set

From 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.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 fibrosis; sarcoidosis, pulmonary Gene Set

From 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.

pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Brain small vessel disease with hemorrhage Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain Small Vessel Disease with Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Vessel Anomalies from the curated CTD Gene-Disease Associations dataset.

vessel stenosis Gene Set

From GAD Gene-Disease Associations

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

cerebral small-vessel disease Gene Set

From GAD Gene-Disease Associations

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

coronary vessel anomalies; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary vessel anomalies; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke, lacunar; small-vessel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vessel Gene Set

From GeneRIF Biological Term Annotations

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

blood vessel endothelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel development biological process from the curated GO Biological Process Annotations dataset.

retinal blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel development biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

labyrinthine layer blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the labyrinthine layer blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration involved in intussusceptive angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration involved in intussusceptive angiogenesis biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel lumenization Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel lumenization biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of testicular blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of testicular blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

placenta blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the placenta blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

lymph vessel development Gene Set

From GO Biological Process Annotations

genes participating in the lymph vessel development biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate specification biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel maturation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

lymph vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the lymph vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

blood vessel Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in blood vessel relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

large vessel vasculitis Gene Set

From HPO Gene-Disease Associations

genes associated with the large vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small vessel vasculitis Gene Set

From HPO Gene-Disease Associations

genes associated with the small vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Coronary Vessel Anomalies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal coronary vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal coronary vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney venous blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney venous blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal afferent lymphatic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal afferent lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel smooth muscle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel smooth muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intersomitic vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intersomitic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel elastic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel elastic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart and great vessel attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart and great vessel attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged lymphatic vessel Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged lymphatic vessel phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lymphatic vessel endothelial cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lymphatic vessel endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney arterial blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney arterial blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal umbilical cord blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal umbilical cord blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urinary bladder blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urinary bladder blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lymphatic vessel hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lymphatic vessel hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymphatic vessel endothelial cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymphatic vessel endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

blood vessel endothelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood vessel endothelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood vessel Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood vessel from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

plant vessel Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue plant vessel from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

plant vessel Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue plant vessel in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

blood vessel endothelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel endothelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

lymph vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue lymph vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

seed vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue seed vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

blood vessel wall Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

blood vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue blood vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

plant vessel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue plant vessel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral portion of GPi Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in peripheral portion of GPi relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

light-harvesting complex, peripheral complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Peripheral Nervous System Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.

Peripheral Vascular Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Vascular Diseases from the curated CTD Gene-Disease Associations dataset.

Neuroectodermal Tumors, Primitive, Peripheral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuroectodermal Tumors, Primitive, Peripheral from the curated CTD Gene-Disease Associations dataset.

Lymphoma, T-Cell, Peripheral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lymphoma, T-Cell, Peripheral from the curated CTD Gene-Disease Associations dataset.

Peripheral Arterial Occlusive Disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Arterial Occlusive Disease 1 from the curated CTD Gene-Disease Associations dataset.

Inherited Peripheral Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inherited Peripheral Neuropathy from the curated CTD Gene-Disease Associations dataset.

peripheral nervous system neoplasm Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease peripheral nervous system neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral vascular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease peripheral vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral primitive neuroectodermal tumor Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease peripheral primitive neuroectodermal tumor from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease peripheral neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of peripheral nervous system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of peripheral nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral nervous system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease peripheral nervous system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral nervous system neoplasm Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease peripheral nervous system neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

peripheral vascular disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease peripheral vascular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

peripheral t-cell lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral t-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autonomic peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral nervous system neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral nervous system neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral vertigo Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of peripheral nervous system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of peripheral nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral nervous system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sensory peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

malignant glandular tumor of peripheral nerve sheath Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease malignant glandular tumor of peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral vascular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral nerve sheath neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral nerve sheath neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral osteosarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epithelioid malignant peripheral nerve sheath tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease epithelioid malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

malignant peripheral nerve sheath tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

motor peripheral neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

peripheral primitive neuroectodermal tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease peripheral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral vascular diseases; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcium homeostasis and peripheral bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral demyelinating neuropathies Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intermittent claudication; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetic neuropathies; peripheral nervous system diseases; sensation disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetic neuropathies; peripheral nervous system diseases; sensation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephropathy in other diseases; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy in other diseases; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; stroke; angina; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; stroke; angina; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

factor vii deficiency; peripheral vascular diseases; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor vii deficiency; peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral vascular diseases; postoperative complications; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease peripheral vascular diseases; postoperative complications; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; intermittent claudication; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; peripheral vascular diseases; vitreous hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; peripheral vascular diseases; vitreous hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; heart failure; myocardial infarction; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; heart failure; myocardial infarction; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemias; myocardial ischemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemias; myocardial ischemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

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

apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; peripheral vascular diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; peripheral vascular diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

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

peripheral vascular diseases; systemic scleroderma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease peripheral vascular diseases; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ischemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peripheral Gene Set

From GeneRIF Biological Term Annotations

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

Peripheral motor neuropathy_Sciatic Nerve_GSE1947 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Peripheral motor neuropathy_Sciatic Nerve_GSE1947 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

peripheral nervous system axon regeneration Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system axon regeneration biological process from the curated GO Biological Process Annotations dataset.

regulation of peripheral tolerance induction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of peripheral tolerance induction biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system myelin formation Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system myelin formation biological process from the curated GO Biological Process Annotations dataset.

myelination in peripheral nervous system Gene Set

From GO Biological Process Annotations

genes participating in the myelination in peripheral nervous system biological process from the curated GO Biological Process Annotations dataset.

renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system neuron development Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system neuron development biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system neuron axonogenesis Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of peripheral tolerance induction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of peripheral tolerance induction biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system myelin maintenance Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system myelin maintenance biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system axon ensheathment Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system axon ensheathment biological process from the curated GO Biological Process Annotations dataset.

positive regulation of peripheral t cell tolerance induction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of peripheral t cell tolerance induction biological process from the curated GO Biological Process Annotations dataset.

regulation of peripheral t cell tolerance induction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of peripheral t cell tolerance induction biological process from the curated GO Biological Process Annotations dataset.

peripheral nervous system development Gene Set

From GO Biological Process Annotations

genes participating in the peripheral nervous system development biological process from the curated GO Biological Process Annotations dataset.

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Peripheral artery disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Peripheral artery disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

peripheral vascular disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease peripheral vascular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

peripheral neuropathy Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

sensory peripheral neuropathy Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease sensory peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

peripheral primitive neuroectodermal tumor Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease peripheral primitive neuroectodermal tumor in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

peripheral nervous system neoplasm Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease peripheral nervous system neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormalities of the peripheral arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormalities of the peripheral arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

peripheral neuropathy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the peripheral neuropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

peripheral primitive neuroectodermal neoplasm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the peripheral primitive neuroectodermal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

peripheral arterial disease Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the peripheral arterial disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

segmental peripheral demyelination/remyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the segmental peripheral demyelination/remyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetrical progressive peripheral demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature peripheral vascular disease Gene Set

From HPO Gene-Disease Associations

genes associated with the premature peripheral vascular disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system synaptic transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral vitreoretinal degeneration Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral retinal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral axonal neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nerves Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral thrombosis Gene Set

From HPO Gene-Disease Associations

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

enlarged peripheral nerve Gene Set

From HPO Gene-Disease Associations

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

abnormal peripheral myelination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral retinopathy Gene Set

From HPO Gene-Disease Associations

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

peripheral schwannoma Gene Set

From HPO Gene-Disease Associations

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

peripheral dysmyelination Gene Set

From HPO Gene-Disease Associations

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

decreased number of small peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral primitive neuroectodermal neoplasm Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral primitive neuroectodermal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

demyelinating peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the demyelinating peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral retinal pigmentation abnormalities Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral retinal pigmentation abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of large peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral arteriovenous fistula Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral arteriovenous fistula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral nerve compression Gene Set

From HPO Gene-Disease Associations

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

progressive peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent microvilli on the surface of peripheral blood lymphocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the absent microvilli on the surface of peripheral blood lymphocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral hypermyelination Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal avascularization Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral retinal avascularization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral axonal atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

delayed peripheral myelination Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormalities of the peripheral arteries Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormalities of the peripheral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral hypomyelination Gene Set

From HPO Gene-Disease Associations

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

episodic peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the episodic peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral vitreous opacities Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral vitreous opacities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral axonal degeneration Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral axonal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral arterial stenosis Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral arterial stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased number of peripheral cd3+ t cells Gene Set

From HPO Gene-Disease Associations

genes associated with the increased number of peripheral cd3+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

segmental peripheral demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the segmental peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased number of peripheral myelinated nerve fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral opacification of the cornea Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral visual field loss Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral demyelination Gene Set

From HPO Gene-Disease Associations

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

distal peripheral sensory neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetric peripheral demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetric peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the peripheral nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the peripheral nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nerve conduction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nerve conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral vascular insufficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral vascular insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neovascularization of peripheral and posterior retina Gene Set

From HPO Gene-Disease Associations

genes associated with the neovascularization of peripheral and posterior retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral traction retinal detachment Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral traction retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral arterial disease Gene Set

From HPO Gene-Disease Associations

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

abnormal peripheral action potential amplitude Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Peripheral Nervous System Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Peripheral Nervous System Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Peripheral Vascular Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Peripheral Vascular Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lymphoma, T-Cell, Peripheral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lymphoma, T-Cell, Peripheral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Peripheral Arterial Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Peripheral Arterial Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Peripheral myelin protein PMP22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peripheral myelin protein PMP22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal peripheral nervous system regeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal peripheral b cell anergy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal peripheral b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal peripheral t cell anergy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal peripheral t cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal peripheral lymph node morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal peripheral lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent peripheral lymph nodes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent peripheral lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

peripheral nervous system degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

peripheral arterial occlusive disease 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the peripheral arterial occlusive disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

agenesis of the corpus callosum with peripheral neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, autosomal dominant, with peripheral neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

peripheral blood mononuclear cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral blood mononuclear cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral blood Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral blood from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral blood lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral blood lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral nerve Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral nerve from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral nervous system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

peripheral nervous system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

peripheral blood Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral blood in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

peripheral primitive neuroectodermal tumor cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral primitive neuroectodermal tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

malignant peripheral nerve sheath cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue malignant peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral blood mononuclear cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral blood mononuclear cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral blood stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral blood stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral blood Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral blood in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral blood cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral blood cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral nerve Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral blood lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral blood lymphocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral nerve sheath cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral nervous system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Renal hypodysplasia/aplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hypodysplasia/aplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Radial aplasia-thrombocytopenia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve aplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital bilateral aplasia of vas deferens Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.

Red-Cell Aplasia, Pure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Red-Cell Aplasia, Pure from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis radial aplasia syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis radial aplasia syndrome from the curated CTD Gene-Disease Associations dataset.

Aplasia of Lacrimal and Salivary Glands Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.

Mullerian Aplasia and Hyperandrogenism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset.

pure red-cell aplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anemia; kidney diseases; red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aplasia Gene Set

From GeneRIF Biological Term Annotations

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

aplasia/hypoplasia involving the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

aplasia/hypoplasia of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

aplasia/hypoplasia of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the inferior half of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita of scalp Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the uterus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lacrimal gland aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lacrimal gland aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the uvula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tragus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the lungs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the quadriceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

biceps aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mandibular aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the scapulae Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the iris Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the middle phalanx of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lacrimal duct aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving forearm bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sternum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ovary Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the corticospinal tracts Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of metacarpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the feet Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita over posterior parietal area Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita over posterior parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the biceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the fundus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the retina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the gallbladder Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of metatarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the uterus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patellar aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the ovary Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the spleen Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplastia of the eccrine sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplastia of the eccrine sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the choroid Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the semicircular canal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mandibular condyle aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the mandibular condyle aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the triceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

quadriceps aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia of the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting bones of the axial skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bilateral radial aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral radial aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the earlobes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 4th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the radius Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the thymus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 2nd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the humerus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the maxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the testes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ribs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 1st metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the metacarpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nipples Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 5th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the diaphragm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the thymus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the premaxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebrum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carpal bone aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the carpal bone aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the bladder Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the uvea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the femur Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the testes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nails Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midclavicular aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia cutis congenita over the scalp vertex Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita over the scalp vertex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the brainstem Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the pectoralis major muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the pectoralis major muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triceps aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the fovea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cochlea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior segment of eye aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the vagina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita on trunk or limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita on trunk or limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the clavicles Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sacrum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the skull Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia involving bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the parotid gland Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tibia Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the patella Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeletal musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eyelid Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the vagina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the breasts Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia involving bones of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia involving bones of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pancreas Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cervical spine Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia involving forearm bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

breast aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the lens Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the external ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the shoulder musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita over parietal area Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tongue Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the colon Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pectoral muscle hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fibular aplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the macula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the musculature of the thigh Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fibula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypodysplasia/aplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal hypodysplasia/aplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

aplasia of lacrimal and salivary glands Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplasia of lacrimal and salivary glands phenotype from the curated OMIM Gene-Disease Associations dataset.

patella aplasia or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the patella aplasia or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?renal hypodysplasia/aplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?renal hypodysplasia/aplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mullerian aplasia and hyperandrogenism Gene Set

From OMIM Gene-Disease Associations

genes associated with the mullerian aplasia and hyperandrogenism phenotype from the curated OMIM Gene-Disease Associations dataset.

aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

?aplasia cutis congenita, nonsyndromic Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?aplasia cutis congenita, nonsyndromic phenotype from the curated OMIM Gene-Disease Associations dataset.

?breasts and/or nipples, aplasia or hypoplasia of, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?breasts and/or nipples, aplasia or hypoplasia of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene Set

From 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.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From 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 arterial hypertension related to hereditary hemorrhagic telangiectasia Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pulmonary alveolar microlithiasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From 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.

Primary pulmonary hypertension 3 Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Familial pulmonary capillary hemangiomatosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pulmonary Surfactants Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Pulmonary Surfactants from the curated CTD Gene-Chemical Interactions dataset.

Pulmonary Embolism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Embolism from the curated CTD Gene-Disease Associations dataset.

Hypertension, Pulmonary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Pulmonary from the curated CTD Gene-Disease Associations dataset.

PULMONARY FUNCTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PULMONARY FUNCTION from the curated CTD Gene-Disease Associations dataset.

Pulmonary Alveolar Microlithiasis Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Emphysema from the curated CTD Gene-Disease Associations dataset.

Pulmonary Eosinophilia Gene Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.

Pulmonary Fibrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.

Anophthalmia with pulmonary hypoplasia Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tuberculosis, Pulmonary from the curated CTD Gene-Disease Associations dataset.

Idiopathic Pulmonary Fibrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene Set

From 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 Set

From 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.

Idiopathic Pulmonary Fibrosis Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

idiopathic pulmonary fibrosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

chronic pulmonary heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease primary pulmonary hypertension from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

pulmonary fibrosis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease pulmonary fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

pulmonary emphysema Gene Set

From DISEASES Experimental Gene-Disease Assocation 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 Set

From DISEASES Experimental Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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.

diffuse pulmonary fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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.

chronic pulmonary heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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.

idiopathic pulmonary fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

pulmonary venoocclusive disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

pulmonary artery leiomyosarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

lung neoplasms; neoplasm of lung ; pulmonary fibrosis Gene Set

From 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 Set

From 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 Set

From 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.

cicatrization; tuberculosis, pulmonary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms Gene Set

From 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.

pulmonary function; nitric oxide; pseudomonas aeruginosa infection Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

chemotherapy-induced pulmonary fibrosis Gene Set

From 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.

aids-related opportunistic infections; tuberculosis; tuberculosis, pulmonary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

fibrosis; pulmonary fibrosis; scleroderma, systemic Gene Set

From 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.

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

From 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 Set

From 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 Set

From 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.

pulmonary fibrosis; sarcoidosis Gene Set

From 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.

thrombosis, deep vein; pulmonary thromboembolism Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

pulmonary fibrosis; scleroderma, systemic Gene Set

From 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.

tuberculosis, multidrug-resistant; tuberculosis, pulmonary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set

From 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.

cardiovascular diseases; pulmonary disease, chronic obstructive Gene Set

From 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 Set

From 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 Set

From 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.

pulmonary fibrosis Gene Set

From 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.

asthma; dermatitis, atopic; chronic obstructive pulmonary disease Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 fibrosis; scleroderma, systemic; systemic scleroderma Gene Set

From 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.

pulmonary thromboembolism Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene Set

From 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 Set

From 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 Set

From 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.

pulmonary tuberculosis Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene Set

From 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.

alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set

From 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.

fibrosis; tuberculosis, pulmonary Gene Set

From 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.

hypertension, pulmonary; kidney diseases; scleroderma, systemic Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

idiopathic pulmonary fibrosis Gene Set

From GAD Gene-Disease Associations

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

chronic obstructive pulmonary disease/copd; emphysema Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From GO Biological Process Annotations

genes participating in the pulmonary valve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

pulmonary vein morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary vein morphogenesis biological process from the curated GO Biological Process Annotations dataset.

pulmonary valve formation Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary valve formation biological process from the curated GO Biological Process Annotations dataset.

pulmonary artery morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary artery morphogenesis biological process from the curated GO Biological Process Annotations dataset.

pulmonary artery endothelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary artery endothelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

pulmonary myocardium development Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary myocardium development biological process from the curated GO Biological Process Annotations dataset.

Idiopathic pulmonary fibrosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Pulmonary function Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

idiopathic pulmonary fibrosis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

pulmonary emphysema Gene Set

From 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 Set

From 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 Set

From GWASdb SNP-Phenotype Associations

genes associated with the pulmonary embolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

pulmonary fibrosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the pulmonary fibrosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased pulmonary function Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

pulmonary infiltrates Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

pulmonary fibrosis Gene Set

From 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.

abnormality of the pulmonary valve Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

abnormal pulmonary lymphatics Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 aterial intimal fibrosis Gene Set

From 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 artery atresia Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Pulmonary Fibrosis Gene Set

From 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.

Sarcoidosis, Pulmonary Gene Set

From 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.

Idiopathic Pulmonary Fibrosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Pulmonary Alveolar Proteinosis Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary hypertension Gene Set

From 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 Set

From 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 Set

From 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 Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pulmonary vein morphology Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.