Name

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

{schistosoma mansoni infection, susceptibility/resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {schistosoma mansoni infection, susceptibility/resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatitis c; schistosoma mansoni infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; schistosoma mansoni infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schistosoma mansoni Gene Set

From GAD Gene-Disease Associations

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

bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytomegalovirus infections; epstein-barr virus infections; herpes simplex; herpes simplex infections; herpesviridae infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; epstein-barr virus infections; herpes simplex; herpes simplex infections; herpesviridae infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytomegalovirus infections; epstein-barr virus infections; polyomavirus infections; recurrence; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; epstein-barr virus infections; polyomavirus infections; recurrence; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; chlamydophila infections; cytomegalovirus infections; enterovirus infections; herpesviridae infections; ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; chlamydophila infections; cytomegalovirus infections; enterovirus infections; herpesviridae infections; ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

burkholderia infections; cystic fibrosis; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burkholderia infections; cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; disease susceptibility; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; disease susceptibility; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

{pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic abscesses due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic iron and fibrosis Gene Set

From GAD Gene-Disease Associations

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

congenital hepatic fibrosis Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic fibrosis Gene Set

From HPO Gene-Disease Associations

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

schistosoma Gene Set

From GeneRIF Biological Term Annotations

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

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

severe combined immunodeficiency due to il2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM 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.

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.

cytomegalovirus infections; flaviviridae infections; hepatitis c; hiv infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; flaviviridae infections; hepatitis c; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; disease susceptibility; lupus erythematosus, systemic; opportunistic infections; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; disease susceptibility; lupus erythematosus, systemic; opportunistic infections; systemic lupus erythematosus 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.

Schistosomiasis mansoni Gene Set

From CTD Gene-Disease Associations

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

schistosomiasis mansoni Gene Set

From GAD Gene-Disease Associations

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

hepatitis c, chronic; schistosomiasis mansoni Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; schistosomiasis mansoni in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mansoni Gene Set

From GeneRIF Biological Term Annotations

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

Schistosomiasis mansoni Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

decreased susceptibility to hepatic steatosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to hepatic steatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset.

alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, severe, susceptibility to, bmiq9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, severe, susceptibility to, bmiq9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{influenza, severe, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {influenza, severe, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, severe, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, severe, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

recurrent infections due to aspiration Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hepatitis due to cryptospridium infection Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{chronic infections, due to mbl deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{thrombophilia, susceptibility to, due to factor v leiden} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset.

cystic fibrosis; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; lung diseases; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; lung diseases; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; diabetes mellitus; pseudomonas infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; diabetes mellitus; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; p. aeruginosa infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; p. aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

{pulmonary fibrosis, idiopathic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{meconium ileus in cystic fibrosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {meconium ileus in cystic fibrosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hiv infections; hiv seropositivity; papillomavirus infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

endocarditis, bacterial; gram-positive bacterial infections; staphylococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endocarditis, bacterial; gram-positive bacterial infections; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus infections; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytomegalovirus infections; herpes simplex; herpes simplex infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; herpes simplex; herpes simplex infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; opportunistic infections; uremia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; opportunistic infections; uremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

herpes simplex; herpes simplex infections; postoperative complications; roseolovirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease herpes simplex; herpes simplex infections; postoperative complications; roseolovirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; recurrence; respiratory tract infections; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; recurrence; respiratory tract infections; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

papillomavirus infections; skin neoplasms; sunburn; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease papillomavirus infections; skin neoplasms; sunburn; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna virus infections; fatty liver; flaviviridae infections; hepatitis, viral, human Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna virus infections; fatty liver; flaviviridae infections; hepatitis, viral, human in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meningococcal infections; pneumococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meningococcal infections; pneumococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; htlv-ii infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; htlv-ii infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacteremia; hiv infections; pneumococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacteremia; hiv infections; pneumococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; multiple myeloma; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, reactive; campylobacter infections; salmonella infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, reactive; campylobacter infections; salmonella infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

laryngeal neoplasm; laryngeal neoplasms; neoplasm recurrence, local; papilloma; papillomavirus infections; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasm recurrence, local; papilloma; papillomavirus infections; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

h. pylori infection; helicobacter pylori infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease h. pylori infection; helicobacter pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacteremia; escherichia coli infections; gram-positive bacterial infections; hypotension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacteremia; escherichia coli infections; gram-positive bacterial infections; hypotension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; hiv infections; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; hiv infections; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infection; hepatitis c infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infection; hepatitis c infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cross infection; pneumonia, ventilator-associated; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cross infection; pneumonia, ventilator-associated; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

burns; disease susceptibility; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burns; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis; disease susceptibility; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis; disease susceptibility; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; disease susceptibility; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hiv infection, susceptibility/resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hiv infection, susceptibility/resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{h. pylori infection, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {h. pylori infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{viral infection, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {viral infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{mycobacterium tuberculosis, susceptibility to infection by} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {mycobacterium tuberculosis, susceptibility to infection by} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hepatitis b virus infection, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatitis b virus infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

Renal-hepatic-pancreatic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hepatic venoocclusive disease with immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hepatic lipase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Porphyria, Acute Hepatic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Porphyria, Acute Hepatic from the curated CTD Gene-Disease Associations dataset.

Hepatic Veno-Occlusive Disease Gene Set

From CTD Gene-Disease Associations

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

Hepatic venoocclusive disease with immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset.

Hepatic Encephalopathy Gene Set

From CTD Gene-Disease Associations

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

RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Hepatic Adenomas, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.

Porphyrias, Hepatic Gene Set

From CTD Gene-Disease Associations

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

Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.

Massive Hepatic Necrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Massive Hepatic Necrosis from the curated CTD Gene-Disease Associations dataset.

Hepatic Insufficiency Gene Set

From CTD Gene-Disease Associations

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

hepatic vein thrombosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic angiomyolipoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic vascular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic coma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic tuberculosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sclerosing hepatic carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic gsta1/gsta2 expression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatic gsta1/gsta2 expression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose, basal hepatic glucose and increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic cyp3a4 expression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatic cyp3a4 expression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lower levels of hepatic lipase activity buoyant ldl and higher hdl2 cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lower levels of hepatic lipase activity buoyant ldl and higher hdl2 cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic veno-occlusive disease Gene Set

From GAD Gene-Disease Associations

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

hepatic encephalopathy; liver cirrhosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatic encephalopathy; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

echinococcosis, hepatic Gene Set

From GAD Gene-Disease Associations

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

low hepatic lipase activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low hepatic lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic artery thrombosis Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hepatic lipase activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hepatic lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic Gene Set

From GeneRIF Biological Term Annotations

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

Hepatic Cirrhosis_Liver_GSE6764 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Hepatic Cirrhosis_Liver_GSE6764 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Hepatic Cirrhosis_Hepatic Tissue_GSE1843 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Hepatic Cirrhosis_Hepatic Tissue_GSE1843 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

regulation of hepatic stellate cell activation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations dataset.

hepatic stellate cell activation Gene Set

From GO Biological Process Annotations

genes participating in the hepatic stellate cell activation biological process from the curated GO Biological Process Annotations dataset.

hepatic duct development Gene Set

From GO Biological Process Annotations

genes participating in the hepatic duct development biological process from the curated GO Biological Process Annotations dataset.

hepatic immune response Gene Set

From GO Biological Process Annotations

genes participating in the hepatic immune response biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hepatic stellate cell activation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations dataset.

hepatic steatosis Gene Set

From GWASdb SNP-Phenotype Associations

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

hepatic granulomatosis Gene Set

From GWASdb SNP-Phenotype Associations

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

acute hepatic failure Gene Set

From HPO Gene-Disease Associations

genes associated with the acute hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic amyloidosis Gene Set

From HPO Gene-Disease Associations

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

increased hepatic glycogen content Gene Set

From HPO Gene-Disease Associations

genes associated with the increased hepatic glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse hepatic steatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

hepatic necrosis Gene Set

From HPO Gene-Disease Associations

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

acute hepatic steatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the acute hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic encephalopathy Gene Set

From HPO Gene-Disease Associations

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

hepatic periportal necrosis Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic periportal necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic calcification Gene Set

From HPO Gene-Disease Associations

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

hepatic steatosis Gene Set

From HPO Gene-Disease Associations

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

malformation of the hepatic ductal plate Gene Set

From HPO Gene-Disease Associations

genes associated with the malformation of the hepatic ductal plate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated hepatic transaminases Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated hepatic transaminases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic vascular malformations Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hepatic vasculature Gene Set

From HPO Gene-Disease Associations

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

hepatic failure Gene Set

From HPO Gene-Disease Associations

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

macrovesicular hepatic steatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the macrovesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic cysts Gene Set

From HPO Gene-Disease Associations

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

fulminant hepatic failure Gene Set

From HPO Gene-Disease Associations

genes associated with the fulminant hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hepatic failure Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

microvesicular hepatic steatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the microvesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hepatic Veno-Occlusive Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hepatic Encephalopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Echinococcosis, Hepatic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Echinococcosis, Hepatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hepatic Vein Thrombosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hepatic Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hepatic leukemia factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hepatic leukemia factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hepatic lipase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hepatic lipase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hepatic lectin, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hepatic lectin, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

multifocal hepatic necrosis Gene Set

From MPO Gene-Phenotype Associations

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

delayed hepatic development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hepatic necrosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hepatic duct morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hepatic diverticulum morphology Gene Set

From MPO Gene-Phenotype Associations

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

hepatic steatosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hepatic portal vein morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hepatic portal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hepatic hemangioma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased hepatic hemangioma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hepatic vein morphology Gene Set

From MPO Gene-Phenotype Associations

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

focal hepatic necrosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hepatic cord morphology Gene Set

From MPO Gene-Phenotype Associations

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

diffuse hepatic necrosis Gene Set

From MPO Gene-Phenotype Associations

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

renal-hepatic-pancreatic dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic venoocclusive disease with immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic venoocclusive disease with immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

porphyria, acute hepatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the porphyria, acute hepatic phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic failure, early onset, and neurologic disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic adenoma, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic adenoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic lipase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic lipase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney and hepatic disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney and hepatic disease phenotype from the curated OMIM Gene-Disease Associations dataset.

cpt deficiency, hepatic, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the cpt deficiency, hepatic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

cpt deficiency, hepatic, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cpt deficiency, hepatic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

?renal-hepatic-pancreatic dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?renal-hepatic-pancreatic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term hepatic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

hepatic stellate cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue hepatic stellate cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

hepatic cecum Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hepatic primordium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hepatic stellate cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hepatic artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hepatic stellate cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

X-linked severe combined immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked severe combined immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency 18, severe combined immunodeficiency variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 18, severe combined immunodeficiency variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperparathyroidism, neonatal severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperparathyroidism, neonatal severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 3, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe X-linked myotubular myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 6, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation 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.

Severe combined immunodeficiency, atypical Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency, atypical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 4, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe myoclonic epilepsy in infancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sialic acid storage disease, severe infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Hyperparathyroidism, Neonatal Severe Primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency from the curated CTD Gene-Disease Associations dataset.

Severe Dengue Gene Set

From CTD Gene-Disease Associations

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

Abnormalities, Severe Teratoid Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abnormalities, Severe Teratoid from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive from the curated CTD Gene-Disease Associations dataset.

Severe Acute Respiratory Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Acute Respiratory Syndrome from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive from the curated CTD Gene-Disease Associations dataset.

Severe combined immunodeficiency with sensitivity to ionizing radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency with sensitivity to ionizing radiation from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked 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.

Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.

severe combined immunodeficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease severe combined immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

severe congenital neutropenia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease severe congenital neutropenia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

severe acute respiratory syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease severe acute respiratory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

severe congenital neutropenia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

severe nonproliferative diabetic retinopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease severe nonproliferative diabetic retinopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

severe combined immunodeficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

severe pre-eclampsia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

severe type iii hyperlipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe type iii hyperlipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyper-ige syndrome and severe eczema. atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-ige syndrome and severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe trauma. mortality Gene Set

From GAD Gene-Disease Associations

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

severe childhood thrombosis Gene Set

From GAD Gene-Disease Associations

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

sars (severe acute respiratory syndrome) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sars (severe acute respiratory syndrome) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyper-ige syndrome. severe eczema. atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-ige syndrome. severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe desmoid phenotype Gene Set

From GAD Gene-Disease Associations

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

mild and severe substance abuse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mild and severe substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe malaria Gene Set

From GAD Gene-Disease Associations

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

communicable diseases; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxemia; anoxia; pneumonia, viral; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe acute radiotherapy side effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe acute radiotherapy side effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe hyperkinetic disorders Gene Set

From GAD Gene-Disease Associations

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

severe sepsis in blunt trauma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe sepsis in blunt trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphopenia; scid; severe combined immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphopenia; scid; severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe ulcerative colitis Gene Set

From GAD Gene-Disease Associations

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

severe sepsis Gene Set

From GAD Gene-Disease Associations

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

bone necrosis; osteonecrosis; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; osteonecrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe chronic neutropenia Gene Set

From GAD Gene-Disease Associations

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

x-linked severe combined immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe rsv bronchiolitis Gene Set

From GAD Gene-Disease Associations

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

outcome after severe injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease outcome after severe injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe sepsis after trauma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe sepsis after trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

immunologic deficiency syndromes; severe combined immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease immunologic deficiency syndromes; severe combined immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe photoaging of facial skin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe Gene Set

From GeneRIF Biological Term Annotations

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

Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

SCID - Severe combined immunodeficiency_Lung Tissue_GSE3414 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during SCID - Severe combined immunodeficiency_Lung Tissue_GSE3414 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Treatment response for severe sepsis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Treatment response for severe sepsis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Acne (severe) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Acne (severe) 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.

Myopia (severe) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Myopia (severe) 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.

Asthma (childhood, severe) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

severe osteoporosis Gene Set

From HPO Gene-Disease Associations

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

severe platyspondyly Gene Set

From HPO Gene-Disease Associations

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

severe photosensitivity Gene Set

From HPO Gene-Disease Associations

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

severe hydrops fetalis Gene Set

From HPO Gene-Disease Associations

genes associated with the severe hydrops fetalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe carpal ossification delay Gene Set

From HPO Gene-Disease Associations

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

severe lactic acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the severe lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe t-cell immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the severe t-cell immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe combined immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the severe combined immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe recurrent varicella Gene Set

From HPO Gene-Disease Associations

genes associated with the severe recurrent varicella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe visual impairment Gene Set

From HPO Gene-Disease Associations

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

intellectual disability, severe Gene Set

From HPO Gene-Disease Associations

genes associated with the intellectual disability, severe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe hydrocephalus Gene Set

From HPO Gene-Disease Associations

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

severe failure to thrive Gene Set

From HPO Gene-Disease Associations

genes associated with the severe failure to thrive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe b lymphocytopenia Gene Set

From HPO Gene-Disease Associations

genes associated with the severe b lymphocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe intrauterine growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the severe intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe short-limb dwarfism Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the severe hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe muscular hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the severe muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe demyelination of the white matter Gene Set

From HPO Gene-Disease Associations

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

severe sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the severe sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe t lymphocytopenia Gene Set

From HPO Gene-Disease Associations

genes associated with the severe t lymphocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe myopia Gene Set

From HPO Gene-Disease Associations

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

severe limb shortening Gene Set

From HPO Gene-Disease Associations

genes associated with the severe limb shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe periodontitis Gene Set

From HPO Gene-Disease Associations

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

severe postnatal growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the severe postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Severe Acute Respiratory Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Severe Acute Respiratory Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Severe Combined Immunodeficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Severe Combined Immunodeficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.

ulna and fibula, absence of, with severe limb deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

insulin resistance, severe, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the insulin resistance, severe, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital 3, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, t cell-negative, b-cell/natural killer-cell positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, t cell-negative, b-cell/natural killer-cell positive phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital, 6, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital, 6, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, neonatal severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, severe, and type ii diabetes} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, severe, and type ii diabetes} phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital, 5, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, severe phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, b cell-negative Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, b cell-negative phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, athabascan type Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, athabascan type phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital 4, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital 4, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary disease, chronic obstructive, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, t-cell negative, b-cell/natural killer cell-positive type Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, t-cell negative, b-cell/natural killer cell-positive type phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, severe, resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, severe, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, severe congenital 2, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, severe congenital 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocysteinemia due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to ficolin 3 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to activated protein C resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset.

Thrombophilia due to Activated Protein C Resistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia due to platelet alloimmunization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pneumoconiosis due to talc Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressed suicide; suicide due to depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

due Gene Set

From GeneRIF Biological Term Annotations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restricted neck movement due to contractures Gene Set

From HPO Gene-Disease Associations

genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic rhinitis due to narrow nasal airway Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weakness due to upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

self-mutilation of tongue and lips due to involuntary movements Gene Set

From HPO Gene-Disease Associations

genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subperiosteal erosions due to secondary hyperparathyroidism Gene Set

From HPO Gene-Disease Associations

genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

painless fractures due to injury Gene Set

From HPO Gene-Disease Associations

genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cellulitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased sweating due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

orthostatic hypotension due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thrombophilia due to hrg deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

nephropathy due to cfhr5 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to heparin cofactor ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, due to ligand-defective apo b Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset.

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

lacticacidemia due to pdx1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

omphalocele due to duplication of 1p31.3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria due to mthfr deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cirrhosis due to liver phosphorylase kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

metachromatic leukodystrophy due to sap-b deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

gigantism due to ghrf hypersecretion Gene Set

From OMIM Gene-Disease Associations

genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

pseudohyperkalemia, familial, 2, due to red cell leak Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, familial, due to decreased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome, due to cox deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome, due to cox deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{drug-induced liver injury due to flucloxacillin} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to activated protein c resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus due to aqueductal stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to elevated hrg Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to elevated hrg phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia due to hb lepore Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

aica-ribosiduria due to atic deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial cox4 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia due to adenosine kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to cytochrome c oxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to ficolin 3 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperfibrinolysis, familial, due to increased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{resistance to malaria due to g6pd deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {resistance to malaria due to g6pd deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemosiderosis, systemic, due to aceruloplasminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to cpt ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema-cirrhosis, due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to myoadenylate deaminase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the Wikipathways Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

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.

Fibrosis of extraocular muscles, congenital, 3b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cystic fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Oral Submucous Fibrosis Gene Set

From CTD Gene-Disease Associations

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

Peritoneal Fibrosis Gene Set

From CTD Gene-Disease Associations

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

Endomyocardial Fibrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Endomyocardial Fibrosis 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.

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.

Cystic Fibrosis Gene Set

From CTD Gene-Disease Associations

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

Fibrosis of Extraocular Muscles, Congenital, 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset.

CYSTIC FIBROSIS, MODIFIER OF, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CYSTIC FIBROSIS, MODIFIER OF, 1 from the curated CTD Gene-Disease Associations dataset.

Fibrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis 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.

Cystic Fibrosis Gene Set

From dbGAP Gene-Trait Associations

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

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.

cystic fibrosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cystic fibrosis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease cystic fibrosis in GWAS datasets from the DISEASES Experimental 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.

cystic fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

oral submucous fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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.

endomyocardial fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

preretinal fibrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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 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.

cholestasis, intrahepatic; fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; ileus; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; ileus; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; lung diseases Gene Set

From GAD Gene-Disease Associations

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

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.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

fibrosis; iron overload Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; diabetes mellitus, type 1; hyperglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; diabetes mellitus, type 1; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

cystic fibrosis; candida Gene Set

From GAD Gene-Disease Associations

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

congenital fibrosis of extraocular muscles type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic diseases; cystic fibrosis; Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; hepatitis c, chronic; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; hepatitis c, chronic; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; liver diseases Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; exocrine pancreatic insufficiency; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis lung disease Gene Set

From GAD Gene-Disease Associations

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

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.

cystic fibrosis; rhinitis; sinusitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; ileus Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; retroperitoneal fibrosis Gene Set

From GAD Gene-Disease Associations

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

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.

cystic fibrosis; pancreatitis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; intussusception Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; fibrosis; mouth neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; fibrosis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung allograft fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; disease models, animal; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; disease models, animal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; hepatitis c Gene Set

From GAD Gene-Disease Associations

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

body weight; cystic fibrosis; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

cystic fibrosis; diabetes complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatty liver; fibrosis; liver diseases Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; urogenital abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; protein-energy malnutrition Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

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

congenital fibrosis of the extraocular muscles Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; maxillary sinusitis; sinusitis, maxillary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; hepatitis c, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; hepatitis b, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; hepatitis b, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

clonorchiasis; fibrosis Gene Set

From GAD Gene-Disease Associations

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

fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis 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.

constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; pancreatitis Gene Set

From GAD Gene-Disease Associations

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

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.

body weight; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; steatorrhea Gene Set

From GAD Gene-Disease Associations

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

fibrosis; lung diseases Gene Set

From GAD Gene-Disease Associations

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

oral submucous fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oral submucous fibrosis; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease oral submucous fibrosis; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; neoplasms; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; hepatitis c, chronic; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; dental caries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; dental caries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; paranasal sinus diseases; sinus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; paranasal sinus diseases; sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aspergillosis; cystic fibrosis; lung diseases, fungal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aspergillosis; cystic fibrosis; lung diseases, fungal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; gastrointestinal diseases Gene Set

From GAD Gene-Disease Associations

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

hcv-induced liver fibrosis Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; growth disorders; nutrition disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; growth disorders; nutrition disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cystic fibrosis; ileus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

cystic fibrosis; Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis. Gene Set

From GAD Gene-Disease Associations

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

fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; fibrosis; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; fibrosis; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; exocrine pancreatic insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrosis; lung diseases, interstitial; scleroderma, systemic Gene Set

From GAD Gene-Disease Associations

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

oral cancer; oral submucous fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease oral cancer; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

fibrosis Gene Set

From GeneRIF Biological Term Annotations

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

Cystic fibrosis severity Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 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.

Hepatitis C induced liver fibrosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

cystic fibrosis Gene Set

From GWASdb SNP-Disease Associations

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

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 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.

tubulointerstitial fibrosis Gene Set

From HPO Gene-Disease Associations

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

pancreatic fibrosis Gene Set

From HPO Gene-Disease Associations

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

myocardial fibrosis Gene Set

From HPO Gene-Disease Associations

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

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.

arterial intimal fibrosis Gene Set

From HPO Gene-Disease Associations

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

congenital fibrosis of extraocular muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

portal fibrosis Gene Set

From HPO Gene-Disease Associations

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

retroperitoneal fibrosis Gene Set

From HPO Gene-Disease Associations

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

perifollicular fibrosis Gene Set

From HPO Gene-Disease Associations

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

endocardial fibrosis Gene Set

From HPO Gene-Disease Associations

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

periportal fibrosis Gene Set

From HPO Gene-Disease Associations

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

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.

Oral Submucous Fibrosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

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.

Cystic Fibrosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

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.

Fibrosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retroperitoneal Fibrosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cystic fibrosis transmembrane conductance regulator Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cystic fibrosis transmembrane conductance regulator protein domain from the InterPro Predicted Protein Domain Annotations dataset.

retinal fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

cardiac interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

cardiac fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

pancreas fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

liver fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

spleen fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

renal fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

perivascular fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the perivascular fibrosis 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.

urinary bladder fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

skeletal muscle interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

skeletal muscle fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

renal glomerulus fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

renal interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

skeletal muscle endomysial fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle endomysial fibrosis 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.

skin fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

{pulmonary fibrosis, telomere-related, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary fibrosis, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

cystic fibrosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystic fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary fibrosis, idiopathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.

fibrosis of extraocular muscles, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fibrosis of extraocular muscles, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

fibrosis of extraocular muscles, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fibrosis of extraocular muscles, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

fibrosis of extraocular muscles, congenital, 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the fibrosis of extraocular muscles, congenital, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

fibrosis of extraocular muscles, congenital, 3a Gene Set

From OMIM Gene-Disease Associations

genes associated with the fibrosis of extraocular muscles, congenital, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.

{cystic fibrosis lung disease, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cystic fibrosis lung disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

fibrosis Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term fibrosis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

cystic fibrosis Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease cystic fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

idiopathic pulmonary fibrosis Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disseminated atypical mycobacterial infection Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disseminated atypical mycobacterial infection phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AIDS-Related Opportunistic Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AIDS-Related Opportunistic Infections from the curated CTD Gene-Disease Associations dataset.

Coronaviridae Infections Gene Set

From CTD Gene-Disease Associations

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

Cytomegalovirus Infections Gene Set

From CTD Gene-Disease Associations

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

Mycobacterium Infections Gene Set

From CTD Gene-Disease Associations

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

Salmonella Infections Gene Set

From CTD Gene-Disease Associations

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

Herpesviridae Infections Gene Set

From CTD Gene-Disease Associations

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

Infection Gene Set

From CTD Gene-Disease Associations

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

Epstein-Barr Virus Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epstein-Barr Virus Infections from the curated CTD Gene-Disease Associations dataset.

Pasteurellaceae Infections Gene Set

From CTD Gene-Disease Associations

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

Gram-Positive Bacterial Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gram-Positive Bacterial Infections from the curated CTD Gene-Disease Associations dataset.

Respiratory Tract Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Tract Infections from the curated CTD Gene-Disease Associations dataset.

Neisseriaceae Infections Gene Set

From CTD Gene-Disease Associations

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

Meningococcal Infections Gene Set

From CTD Gene-Disease Associations

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

Central Nervous System Infections Gene Set

From CTD Gene-Disease Associations

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

Flavivirus Infections Gene Set

From CTD Gene-Disease Associations

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

Helicobacter Infections Gene Set

From CTD Gene-Disease Associations

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

Streptococcal Infections Gene Set

From CTD Gene-Disease Associations

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

Chlamydia Infections Gene Set

From CTD Gene-Disease Associations

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

Mycoplasma Infections Gene Set

From CTD Gene-Disease Associations

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

Salmonella Infections, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Salmonella Infections, Animal from the curated CTD Gene-Disease Associations dataset.

Staphylococcal Infections Gene Set

From CTD Gene-Disease Associations

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

Escherichia coli Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Escherichia coli Infections from the curated CTD Gene-Disease Associations dataset.

Enterovirus Infections Gene Set

From CTD Gene-Disease Associations

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

Urinary Tract Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Urinary Tract Infections from the curated CTD Gene-Disease Associations dataset.

Coxsackievirus Infections Gene Set

From CTD Gene-Disease Associations

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

Respiratory Syncytial Virus Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Syncytial Virus Infections from the curated CTD Gene-Disease Associations dataset.

PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL from the curated CTD Gene-Disease Associations dataset.

Gram-Negative Bacterial Infections Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gram-Negative Bacterial Infections from the curated CTD Gene-Disease Associations dataset.

Pneumococcal Infections Gene Set

From CTD Gene-Disease Associations

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

HIV Infections Gene Set

From CTD Gene-Disease Associations

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

Papillomavirus Infections Gene Set

From CTD Gene-Disease Associations

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

Caliciviridae Infections Gene Set

From CTD Gene-Disease Associations

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

Pseudomonas Infections Gene Set

From CTD Gene-Disease Associations

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

Haemophilus Infections Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Mycobacterium Infections, Nontuberculous Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mycobacterium Infections, Nontuberculous from the curated CTD Gene-Disease Associations dataset.

Cardiovirus Infections Gene Set

From CTD Gene-Disease Associations

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

Proteus Infections Gene Set

From CTD Gene-Disease Associations

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

Arenaviridae Infections Gene Set

From CTD Gene-Disease Associations

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

Bacterial Infections Gene Set

From CTD Gene-Disease Associations

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

Eye Infections, Bacterial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Eye Infections, Bacterial from the curated CTD Gene-Disease Associations dataset.

Rickettsia Infections Gene Set

From CTD Gene-Disease Associations

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

Meningococcal Infections Gene Set

From dbGAP Gene-Trait Associations

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

bacteriuria; urinary tract infection; urinary tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacteriuria; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal ulcer; gastritis; helicobacter infections; stomach neoplasms; stomach ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal ulcer; gastritis; helicobacter infections; stomach neoplasms; stomach ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; conjunctival neoplasms; hiv infections; squamous cell carcinoma; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; conjunctival neoplasms; hiv infections; squamous cell carcinoma; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

gastritis; helicobacter infections; metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; thrombosis Gene Set

From GAD Gene-Disease Associations

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

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; hiv seropositivity; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

community-acquired infections; pneumonia, bacterial; pneumonia, viral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, viral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; liver cirrhosis; peptic ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; liver cirrhosis; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory syncytial virus infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory syncytial virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; cocarcinogenesis; mouth neoplasms; papillomavirus infections; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cocarcinogenesis; mouth neoplasms; papillomavirus infections; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; recurrence; respiratory sounds; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; recurrence; respiratory sounds; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

sepsis; systemic infection; wounds, nonpenetrating Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sepsis; systemic infection; wounds, nonpenetrating in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cancer; hiv infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cancer; hiv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; papillomavirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; kidney failure, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; kidney failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

community-acquired infections; pneumonia, bacterial; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease community-acquired infections; pneumonia, bacterial; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; gastritis; helicobacter infections; metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, squamous cell; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, squamous cell; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; hiv infections; hiv-associated lipodystrophy syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; hiv infections; hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; infectious mononucleosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; infectious mononucleosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parasitic infection Gene Set

From GAD Gene-Disease Associations

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

cadaver; cytomegalovirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; cytomegalovirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter pylori infection. Gene Set

From GAD Gene-Disease Associations

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

hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

common cold; otitis media; picornaviridae infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease common cold; otitis media; picornaviridae infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, squamous cell; papillomavirus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, squamous cell; papillomavirus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent bacterial infections Gene Set

From GAD Gene-Disease Associations

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

human papillomavirus infection Gene Set

From GAD Gene-Disease Associations

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

pneumococcal infections Gene Set

From GAD Gene-Disease Associations

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

carcinoma; cervical neoplasm; papillomavirus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; cervical neoplasm; papillomavirus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chlamydia infections; macular degeneration Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; papillomavirus infections; penile neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; papillomavirus infections; penile neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; liver failure; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; liver failure; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiolitis, viral; respiratory syncytial virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiolitis, viral; respiratory syncytial virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids-related opportunistic infections; herpes genitalis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; herpes genitalis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal diseases; helicobacter infections; stomach diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal diseases; helicobacter infections; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug eruptions; hiv infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug eruptions; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophagitis, peptic; gastritis; helicobacter infections; peptic esophagitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophagitis, peptic; gastritis; helicobacter infections; peptic esophagitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; lymphohistiocytosis, hemophagocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; lymphohistiocytosis, hemophagocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; viremia; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

malaria infection Gene Set

From GAD Gene-Disease Associations

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

gram-negative bacterial infections; neutropenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gram-negative bacterial infections; neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; hiv-associated lipodystrophy syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; hiv-associated lipodystrophy syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; candidiasis, cutaneous; cutaneous candidiasis; cytomegalovirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; candidiasis, cutaneous; cutaneous candidiasis; cytomegalovirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections; squamous cell carcinoma; tumor of oropharynx Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections; squamous cell carcinoma; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; precancerous conditions; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacteremia; leucocytosis; leukocytosis; staphylococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacteremia; leucocytosis; leukocytosis; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

h. pylori infection; stomach cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease h. pylori infection; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis; helicobacter infections; stomach ulcer; stomach; ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; helicobacter infections; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b; hepatitis c; hiv infections; porphyria cutanea tarda; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b; hepatitis c; hiv infections; porphyria cutanea tarda; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; gastritis; helicobacter infections; metaplasia; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; gastritis; helicobacter infections; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; tuberculosis; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

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

helicobacter infections; stomach ulcer; stomach; ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv/siv infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv/siv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; hiv infections; liver cirrhosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; hiv infections; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; hypersensitivity; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; hypersensitivity; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

papillomavirus infections; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease papillomavirus infections; uterine cervical 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.

atrophy; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical neoplasm; papillomavirus infections; precancerous conditions; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical neoplasm; papillomavirus infections; precancerous conditions; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; infant, newborn, diseases; infection; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; gastritis; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypercholesterolemia; h. pylori infection; coagulation disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypercholesterolemia; h. pylori infection; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; lymphoproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parvovirus b19 infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parvovirus b19 infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis, atrophic; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis, atrophic; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; helicobacter infections; peptic ulcer; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; helicobacter infections; peptic ulcer; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

furunculosis; staphylococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease furunculosis; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cross infection; pneumonia, ventilator-associated; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cross infection; pneumonia, ventilator-associated; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal ulcer; gastritis; helicobacter infections; metaplasia; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal ulcer; gastritis; helicobacter infections; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cross infection; hepatitis b; hepatitis c; hiv infections; hiv seropositivity; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cross infection; hepatitis b; hepatitis c; hiv infections; hiv seropositivity; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; hodgkin disease; pseudolymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; hodgkin disease; pseudolymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; mycobacterium avium-intracellulare infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; enterovirus infections Gene Set

From GAD Gene-Disease Associations

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

atrophy; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasmodium falciparum infection Gene Set

From GAD Gene-Disease Associations

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

alphavirus infections; arthralgia; paraplegia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alphavirus infections; arthralgia; paraplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; hematologic neoplasms; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; hematologic neoplasms; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical intraepithelial neoplasia; papillomavirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical intraepithelial neoplasia; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pancreatitis; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pancreatitis; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

h. pylori infection Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal ulcer; gastrointestinal diseases; helicobacter infections; stomach neoplasms; stomach ulcer; stomach; ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal ulcer; gastrointestinal diseases; helicobacter infections; stomach neoplasms; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastroesophageal reflux; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastroesophageal reflux; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; helicobacter infections; precancerous conditions; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; esophageal neoplasms; helicobacter infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

staphylococcal infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease staphylococcal infection 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.

asthma; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; hiv infections Gene Set

From GAD Gene-Disease Associations

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

ascaris infection Gene Set

From GAD Gene-Disease Associations

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

asthma; helicobacter infections; hypersensitivity, immediate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; helicobacter infections; hypersensitivity, immediate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal ulcer; gastritis; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal ulcer; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.