Name

{bronchiectasis with or without elevated sweat chloride 1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bronchiectasis with or without elevated sweat chloride 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

Bronchiectasis with or without elevated sweat chloride 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis with or without elevated sweat chloride 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 1 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 2 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 3 from the curated CTD Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

elevated sweat chloride concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated sweat chloride concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated sweat chloride Gene Set

From HPO Gene-Disease Associations

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

sweat chloride elevation without cf Gene Set

From OMIM Gene-Disease Associations

genes associated with the sweat chloride elevation without cf phenotype from the curated OMIM Gene-Disease Associations dataset.

Bronchiectasis Gene Set

From ClinVar Gene-Phenotype Associations

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

Bronchiectasis Gene Set

From CTD Gene-Disease Associations

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

bronchiectasis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bronchiectasis; bronchitis; bronchitis unspecified; emphysema; lung diseases, obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiectasis; bronchitis; bronchitis unspecified; emphysema; lung diseases, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiectasis; immunologic deficiency syndromes Gene Set

From GAD Gene-Disease Associations

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

bronchiectasis; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

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

bronchiectasis; common variable immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchiectasis; common variable immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchiectasis; Gene Set

From GAD Gene-Disease Associations

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

obstructive pulmonary disease and disseminated bronchiectasis Gene Set

From GAD Gene-Disease Associations

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

familial bronchiectasis. Gene Set

From GAD Gene-Disease Associations

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

asthma; bronchiectasis Gene Set

From GAD Gene-Disease Associations

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

bronchiectasis Gene Set

From GAD Gene-Disease Associations

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

bronchiectasis Gene Set

From GeneRIF Biological Term Annotations

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

bronchiectasis Gene Set

From HPO Gene-Disease Associations

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

Bronchiectasis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

bronchiectasis Gene Set

From MPO Gene-Phenotype Associations

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

DEAFNESS, NONSYNDROMIC, MODIFIER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, NONSYNDROMIC, MODIFIER 1 from the curated CTD Gene-Disease Associations dataset.

VAN DER WOUDE SYNDROME 1, MODIFIER OF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VAN DER WOUDE SYNDROME 1, MODIFIER OF 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.

modifier Gene Set

From GeneRIF Biological Term Annotations

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

clinical modifier Gene Set

From GWASdb SNP-Phenotype Associations

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

clinical modifier Gene Set

From HPO Gene-Disease Associations

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

Ubiquitin-fold modifier 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin-fold modifier 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Modifier of rudimentary, Modr Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Modifier of rudimentary, Modr protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C78, ubiquitin fold modifier-specific peptidase 1/ 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C78, ubiquitin fold modifier-specific peptidase 1/ 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin-fold modifier-conjugating enzyme 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin-fold modifier-conjugating enzyme 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin-related modifier 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin-related modifier 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small ubiquitin-related modifier, chordates Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small ubiquitin-related modifier, chordates protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin-like modifier-activating enzyme Atg7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin-like modifier-activating enzyme Atg7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{von hippel-lindau syndrome, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {von hippel-lindau syndrome, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{bardet-biedl syndrome 14, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bardet-biedl syndrome 14, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{albinism, oculocutaneous, type ii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {albinism, oculocutaneous, type ii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hfe hemochromatosis, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hfe hemochromatosis, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, nonsyndromic, modifier 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, nonsyndromic, modifier 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pheochromocytoma, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pheochromocytoma, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epidermolysis bullosa dystrophica, autosomal recessive, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epidermolysis bullosa dystrophica, autosomal recessive, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dystonia-1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dystonia-1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{tsc2 angiomyolipomas, renal, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {tsc2 angiomyolipomas, renal, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, disease progression, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, disease progression, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, mitochondrial, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, mitochondrial, modifier of} 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.

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, autosomal recessive 12, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, autosomal recessive 12, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{bardet-biedl syndrome 1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bardet-biedl syndrome 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{congestive heart failure and beta-blocker response, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {congestive heart failure and beta-blocker response, modifier of} 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.

{centronuclear myopathy, autosomal, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {centronuclear myopathy, autosomal, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{46xy sex reversal 8, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {46xy sex reversal 8, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, modifier of} Gene Set

From OMIM Gene-Disease Associations

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

{pseudoxanthoma elasticum, modifier of severity of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pseudoxanthoma elasticum, modifier of severity of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{dravet syndrome, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dravet syndrome, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

Sweat Gland Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sweat Gland Neoplasms from the curated CTD Gene-Disease Associations dataset.

sweat gland disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

sweat gland carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eccrine sweat gland neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sweat gland cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eccrine sweat gland cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease eccrine sweat gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

apocrine sweat gland neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sweat gland disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

apocrine sweat gland cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease apocrine sweat gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sweat gland neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sweat gland diseases Gene Set

From GAD Gene-Disease Associations

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

sweat Gene Set

From GeneRIF Biological Term Annotations

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

decreased number of sweat glands Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplastia of the eccrine sweat glands Gene Set

From HPO Gene-Disease Associations

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

abnormal sweat homeostasis Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

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

aplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sweat gland Gene Set

From HPO Gene-Disease Associations

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

Sweat Gland Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal sweat gland morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sweat gland physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sweat gland secretion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sweat gland secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sweat gland Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

eccrine sweat gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

apocrine sweat gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

sweat gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

sweat Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

rostral division of OFCi (area 11) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral division of OFCi (area 11) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

ofloxacin-2340 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ofloxacin-2340 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ofloxacin-2302 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ofloxacin-2302 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ofloxacin-7372 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ofloxacin-7372 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ofloxacin-3673 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ofloxacin-3673 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ofloxacin-4696 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ofloxacin-4696 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Ofloxacin Gene Set

From CTD Gene-Chemical Interactions

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

specific bursitis often of occupational origin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease specific bursitis often of occupational origin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Ofloxacin Gene Set

From DrugBank Drug Targets

interacting proteins for the Ofloxacin drug from the curated DrugBank Drug Targets dataset.

violent offenders with mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease violent offenders with mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ofc Gene Set

From GeneRIF Biological Term Annotations

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

off Gene Set

From GeneRIF Biological Term Annotations

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

ofr Gene Set

From GeneRIF Biological Term Annotations

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

of1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term of1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ofd Gene Set

From GeneRIF Biological Term Annotations

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

offspring Gene Set

From GeneRIF Biological Term Annotations

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

offer Gene Set

From GeneRIF Biological Term Annotations

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

ofor Gene Set

From GeneRIF Biological Term Annotations

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

officers Gene Set

From GeneRIF Biological Term Annotations

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

ofbetacatenin Gene Set

From GeneRIF Biological Term Annotations

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

offpathway Gene Set

From GeneRIF Biological Term Annotations

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

officinalis Gene Set

From GeneRIF Biological Term Annotations

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

ofalzheimer Gene Set

From GeneRIF Biological Term Annotations

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

office Gene Set

From GeneRIF Biological Term Annotations

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

ofucose Gene Set

From GeneRIF Biological Term Annotations

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

offering Gene Set

From GeneRIF Biological Term Annotations

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

ofpaediatric Gene Set

From GeneRIF Biological Term Annotations

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

offtarget Gene Set

From GeneRIF Biological Term Annotations

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

ofucosylation Gene Set

From GeneRIF Biological Term Annotations

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

oftrpv14 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term oftrpv14 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ofthe Gene Set

From GeneRIF Biological Term Annotations

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

offon Gene Set

From GeneRIF Biological Term Annotations

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

ofqnociceptin Gene Set

From GeneRIF Biological Term Annotations

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

offpump Gene Set

From GeneRIF Biological Term Annotations

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

ofalphasynuclein Gene Set

From GeneRIF Biological Term Annotations

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

ofuterine Gene Set

From GeneRIF Biological Term Annotations

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

ofmt Gene Set

From GeneRIF Biological Term Annotations

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

offered Gene Set

From GeneRIF Biological Term Annotations

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

ofucosyltransferase Gene Set

From GeneRIF Biological Term Annotations

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

often Gene Set

From GeneRIF Biological Term Annotations

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

officially Gene Set

From GeneRIF Biological Term Annotations

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

offrate Gene Set

From GeneRIF Biological Term Annotations

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

offsprings Gene Set

From GeneRIF Biological Term Annotations

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

offers Gene Set

From GeneRIF Biological Term Annotations

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

offenders Gene Set

From GeneRIF Biological Term Annotations

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

official Gene Set

From GeneRIF Biological Term Annotations

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

offset Gene Set

From GeneRIF Biological Term Annotations

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

ofankk1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ofankk1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ofd1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ofd1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ofendothelial Gene Set

From GeneRIF Biological Term Annotations

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

[Arg14Lys15]N/OFQ Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Arg14Lys15]N/OFQ ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

N/OFQ-(1-13)-NH2 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the N/OFQ-(1-13)-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[(pF)Phe4]N/OFQ-(1-13)-NH2 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [(pF)Phe4]N/OFQ-(1-13)-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ofatumumab Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ofatumumab ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[3H]N/OFQ Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [3H]N/OFQ ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[3H]Tyr14-N/OFQ Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [3H]Tyr14-N/OFQ ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

N/OFQ-NH2 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the N/OFQ-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Nphe1]N/OFQ-(1-13)-NH2 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Nphe1]N/OFQ-(1-13)-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[F/G]N/OFQ-(1-13)-NH2 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [F/G]N/OFQ-(1-13)-NH2 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Ofloxacin Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Ofloxacin metabolite from the curated HMDB Metabolites of Enzymes dataset.

flattened, squared-off epiphyses of tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the flattened, squared-off epiphyses of tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal offspring retrieval Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal offspring retrieval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

OFD1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for OFD1 from the Pathway Commons Protein-Protein Interactions dataset.

OFCC1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for OFCC1 from the Pathway Commons Protein-Protein Interactions dataset.

Hedgehog 'off' state Gene Set

From Reactome Pathways

proteins participating in the Hedgehog 'off' state pathway from the Reactome Pathways dataset.

Superoxide dismutase, elevated extracellular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Superoxide dismutase, elevated extracellular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenosine triphosphate, elevated, of erythrocytes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenosine triphosphate, elevated, of erythrocytes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CREATINE PHOSPHOKINASE, ELEVATED SERUM Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CREATINE PHOSPHOKINASE, ELEVATED SERUM from the curated CTD Gene-Disease Associations dataset.

Adenosine Triphosphate, Elevated, Of Erythrocytes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenosine Triphosphate, Elevated, Of Erythrocytes 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.

ZINC, ELEVATED PLASMA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ZINC, ELEVATED PLASMA from the curated CTD Gene-Disease Associations dataset.

elevated apo b levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated apo b levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated hdl cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated hdl cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated ace Gene Set

From GAD Gene-Disease Associations

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

elevated liver enzymes and metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated liver enzymes and metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated fasting blood glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated fasting blood glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated response to ghrh by pituitary somatotrophinomas Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated response to ghrh by pituitary somatotrophinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated serum apolipoprotein ai levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated serum apolipoprotein ai levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated plasma prothrombin levels and an increase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated plasma prothrombin levels and an increase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced cbs activity and elevated post-load homocysteine levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced cbs activity and elevated post-load homocysteine levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated blood pressure and personality disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated blood pressure and personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cortisol escape from dexamethasone and elevated glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cortisol escape from dexamethasone and elevated glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated Gene Set

From GeneRIF Biological Term Annotations

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

Elevated serum carcinoembryonic antigen levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Elevated serum carcinoembryonic antigen levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

elevated follicle stimulating hormone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the elevated follicle stimulating hormone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

elevated systolic blood pressure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the elevated systolic blood pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

elevated urinary epinephrine Gene Set

From HPO Gene-Disease Associations

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

elevated serum creatine phosphokinase Gene Set

From HPO Gene-Disease Associations

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

elevated urinary homovanillic acid Gene Set

From HPO Gene-Disease Associations

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

elevated serum creatinine Gene Set

From HPO Gene-Disease Associations

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

elevated 8-dehydrocholesterol Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated 8-dehydrocholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated levels of phytanic acid Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated levels of phytanic acid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mildly elevated creatine phosphokinase Gene Set

From HPO Gene-Disease Associations

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

elevated urinary dopamine Gene Set

From HPO Gene-Disease Associations

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

elevated intracellular cystine Gene Set

From HPO Gene-Disease Associations

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

elevated 7-dehydrocholesterol Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated 7-dehydrocholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated erythrocyte sedimentation rate Gene Set

From HPO Gene-Disease Associations

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

elevated diastolic blood pressure Gene Set

From HPO Gene-Disease Associations

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

elevated follicle stimulating hormone Gene Set

From HPO Gene-Disease Associations

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

elevated amniotic fluid alpha-fetoprotein Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated amniotic fluid alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated 8(9)-cholestenol Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated 8(9)-cholestenol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated alpha-fetoprotein Gene Set

From HPO Gene-Disease Associations

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

elevated c-reactive protein level Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated c-reactive protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated systolic blood pressure Gene Set

From HPO Gene-Disease Associations

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

elevated right atrial pressure Gene Set

From HPO Gene-Disease Associations

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

elevated leukocyte alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

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

elevated urinary vanillylmandelic acid Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated urinary vanillylmandelic acid 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.

elevated urinary delta-aminolevulinic acid Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated urinary delta-aminolevulinic acid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated long chain fatty acids Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated long chain fatty acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

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

elevated urinary norepinephrine Gene Set

From HPO Gene-Disease Associations

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

elevated serum acid phosphatase Gene Set

From HPO Gene-Disease Associations

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

elevated plasma branched chain amino acids Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated plasma branched chain amino acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated mean arterial pressure Gene Set

From HPO Gene-Disease Associations

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

elevated calcitonin Gene Set

From HPO Gene-Disease Associations

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

elevated serum transaminases during infections Gene Set

From HPO Gene-Disease Associations

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

elevated circulating catecholamine level Gene Set

From HPO Gene-Disease Associations

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

elevated circulating parathyroid hormone (pth) level Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated circulating parathyroid hormone (pth) level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated tissue non-specific alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated tissue non-specific alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated plasma citrulline Gene Set

From HPO Gene-Disease Associations

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

elevated alkaline phosphatase of bone origin Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated alkaline phosphatase of bone origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated maternal serum alpha-fetoprotein Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated maternal serum alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated urinary catecholamines Gene Set

From HPO Gene-Disease Associations

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

elevated urine pyrophosphate Gene Set

From HPO Gene-Disease Associations

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

elevated pulmonary artery pressure Gene Set

From HPO Gene-Disease Associations

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

elevated plasma pyrophosphate Gene Set

From HPO Gene-Disease Associations

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

elevated level of mitotic sister chromatid exchange Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the elevated level of mitotic sister chromatid exchange phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

adenosine triphosphate, elevated, of erythrocytes Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenosine triphosphate, elevated, of erythrocytes phenotype from the curated OMIM Gene-Disease Associations dataset.

[superoxide dismutase, elevated extracellular] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [superoxide dismutase, elevated extracellular] phenotype from the curated OMIM Gene-Disease Associations dataset.

creatine phosphokinase, elevated serum Gene Set

From OMIM Gene-Disease Associations

genes associated with the creatine phosphokinase, elevated serum phenotype from the curated OMIM Gene-Disease Associations dataset.

[ige, elevated level of] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [ige, elevated level of] 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.

homocysteine, total plasma, elevated Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocysteine, total plasma, elevated phenotype from the curated OMIM Gene-Disease Associations dataset.

Response to elevated platelet cytosolic Ca2+ Gene Set

From Reactome Pathways

proteins participating in the Response to elevated platelet cytosolic Ca2+ pathway from the Reactome Pathways dataset.

deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling Gene Set

From Reactome Pathways

proteins participating in the deletions in the AXIN genes in hepatocellular carcinoma result in elevated WNT signaling pathway from the Reactome Pathways dataset.

Congenital secretory diarrhea, chloride type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

tubocurarine chloride-5449 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tubocurarine chloride-5449 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methacholine chloride-5773 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methacholine chloride-5773 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tubocurarine chloride-6351 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tubocurarine chloride-6351 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-3850 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-3850 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alcuronium chloride-4409 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alcuronium chloride-4409 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-2190 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-2190 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

edrophonium chloride-1519 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the edrophonium chloride-1519 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-3768 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-3768 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

benzethonium chloride-2508 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the benzethonium chloride-2508 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-4325 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-4325 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cobalt chloride-379 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cobalt chloride-379 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dequalinium chloride-1276 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dequalinium chloride-1276 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tubocurarine chloride-1738 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tubocurarine chloride-1738 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alcuronium chloride-7345 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alcuronium chloride-7345 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

edrophonium chloride-6655 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the edrophonium chloride-6655 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cobalt chloride-454 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cobalt chloride-454 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methacholine chloride-6248 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methacholine chloride-6248 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

benzethonium chloride-6070 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the benzethonium chloride-6070 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

benzethonium chloride-7207 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the benzethonium chloride-7207 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dequalinium chloride-2631 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dequalinium chloride-2631 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

edrophonium chloride-2019 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the edrophonium chloride-2019 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-3943 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-3943 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

edrophonium chloride-5001 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the edrophonium chloride-5001 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

edrophonium chloride-1936 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the edrophonium chloride-1936 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tubocurarine chloride-2887 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tubocurarine chloride-2887 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-6045 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-6045 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dequalinium chloride-6296 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dequalinium chloride-6296 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methacholine chloride-3452 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methacholine chloride-3452 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dequalinium chloride-5396 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dequalinium chloride-5396 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cobalt chloride-383 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cobalt chloride-383 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chloride channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chloride channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chloride channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

glycine-gated chloride channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the glycine-gated chloride channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Methacholine Chloride Gene Set

From CTD Gene-Chemical Interactions

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

trityl chloride Gene Set

From CTD Gene-Chemical Interactions

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

ferric chloride Gene Set

From CTD Gene-Chemical Interactions

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

Cadmium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

stannous chloride Gene Set

From CTD Gene-Chemical Interactions

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

Sodium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

phenylalanyl-prolyl-arginine methyl chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical phenylalanyl-prolyl-arginine methyl chloride from the curated CTD Gene-Chemical Interactions dataset.

ferrous chloride Gene Set

From CTD Gene-Chemical Interactions

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

(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical (4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride from the curated CTD Gene-Chemical Interactions dataset.

5-butyl-6-hydroxy-10-chlorobenzo(c)quinolizinium chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5-butyl-6-hydroxy-10-chlorobenzo(c)quinolizinium chloride from the curated CTD Gene-Chemical Interactions dataset.

phosphoryl chloride Gene Set

From CTD Gene-Chemical Interactions

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

benzoyl chloride Gene Set

From CTD Gene-Chemical Interactions

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

methylmercuric chloride Gene Set

From CTD Gene-Chemical Interactions

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

diphenyltin chloride Gene Set

From CTD Gene-Chemical Interactions

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

Ambenonium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

Obidoxime Chloride Gene Set

From CTD Gene-Chemical Interactions

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

5,10,15,20-(etra(N-methyl-3-pyridyl))-26,28-diselenasapphyrin chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5,10,15,20-(etra(N-methyl-3-pyridyl))-26,28-diselenasapphyrin chloride from the curated CTD Gene-Chemical Interactions dataset.

palladium chloride Gene Set

From CTD Gene-Chemical Interactions

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

Lithium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

4-nitrobenzyl chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 4-nitrobenzyl chloride from the curated CTD Gene-Chemical Interactions dataset.

phenylmercuric chloride Gene Set

From CTD Gene-Chemical Interactions

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

triphenylphosphine gold chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical triphenylphosphine gold chloride from the curated CTD Gene-Chemical Interactions dataset.

allyl chloride Gene Set

From CTD Gene-Chemical Interactions

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

Sodium Chloride Symporter Inhibitors Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Sodium Chloride Symporter Inhibitors from the curated CTD Gene-Chemical Interactions dataset.

Picryl Chloride Gene Set

From CTD Gene-Chemical Interactions

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

phosphorus chloride Gene Set

From CTD Gene-Chemical Interactions

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

cesium chloride Gene Set

From CTD Gene-Chemical Interactions

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

5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride from the curated CTD Gene-Chemical Interactions dataset.

asoxime chloride Gene Set

From CTD Gene-Chemical Interactions

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

chromic chloride Gene Set

From CTD Gene-Chemical Interactions

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

Ammonium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

strontium chloride Gene Set

From CTD Gene-Chemical Interactions

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

methionylmethylsulfonium chloride Gene Set

From CTD Gene-Chemical Interactions

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

Magnesium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

Sodium Chloride, Dietary Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Sodium Chloride, Dietary from the curated CTD Gene-Chemical Interactions dataset.

Methylene Chloride Gene Set

From CTD Gene-Chemical Interactions

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

lanthanum chloride Gene Set

From CTD Gene-Chemical Interactions

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

gold chloride Gene Set

From CTD Gene-Chemical Interactions

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

triphenyltin chloride Gene Set

From CTD Gene-Chemical Interactions

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

gadolinium chloride Gene Set

From CTD Gene-Chemical Interactions

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

cuprous chloride Gene Set

From CTD Gene-Chemical Interactions

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

barium chloride Gene Set

From CTD Gene-Chemical Interactions

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

Calcium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

cupric chloride Gene Set

From CTD Gene-Chemical Interactions

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

Potassium Chloride Gene Set

From CTD Gene-Chemical Interactions

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

manganese chloride Gene Set

From CTD Gene-Chemical Interactions

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

vinylidene chloride Gene Set

From CTD Gene-Chemical Interactions

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

tris(1,10-phenanthroline)chromium(III) chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical tris(1,10-phenanthroline)chromium(III) chloride from the curated CTD Gene-Chemical Interactions dataset.

Vinyl Chloride Gene Set

From CTD Gene-Chemical Interactions

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

chromous chloride Gene Set

From CTD Gene-Chemical Interactions

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

silver chloride Gene Set

From CTD Gene-Chemical Interactions

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

Mercuric Chloride Gene Set

From CTD Gene-Chemical Interactions

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

zinc chloride Gene Set

From CTD Gene-Chemical Interactions

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

aluminum chloride Gene Set

From CTD Gene-Chemical Interactions

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

Methyl Chloride Gene Set

From CTD Gene-Chemical Interactions

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

trimethyltin chloride Gene Set

From CTD Gene-Chemical Interactions

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

nickel chloride Gene Set

From CTD Gene-Chemical Interactions

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

molybdenum chloride Gene Set

From CTD Gene-Chemical Interactions

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

cobaltous chloride Gene Set

From CTD Gene-Chemical Interactions

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

lead chloride Gene Set

From CTD Gene-Chemical Interactions

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

Ethylmercuric Chloride Gene Set

From CTD Gene-Chemical Interactions

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

cerous chloride Gene Set

From CTD Gene-Chemical Interactions

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

Doxacurium chloride Gene Set

From DrugBank Drug Targets

interacting proteins for the Doxacurium chloride drug from the curated DrugBank Drug Targets dataset.

2-(2f-Benzothiazolyl)-5-Styryl-3-(4f-Phthalhydrazidyl)Tetrazolium Chloride Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-(2f-Benzothiazolyl)-5-Styryl-3-(4f-Phthalhydrazidyl)Tetrazolium Chloride drug from the curated DrugBank Drug Targets dataset.

Potassium Chloride Gene Set

From DrugBank Drug Targets

interacting proteins for the Potassium Chloride drug from the curated DrugBank Drug Targets dataset.

vinyl chloride Gene Set

From GAD Gene-Disease Associations

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

vinyl chloride monomer-exposure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vinyl chloride monomer-exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vinyl chloride exposure Gene Set

From GAD Gene-Disease Associations

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

chloride Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of chloride transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of chloride transport biological process from the curated GO Biological Process Annotations dataset.

regulation of intracellular calcium activated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intracellular calcium activated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

chloride transmembrane transport Gene Set

From GO Biological Process Annotations

genes participating in the chloride transmembrane transport biological process from the curated GO Biological Process Annotations dataset.

chloride transport Gene Set

From GO Biological Process Annotations

genes participating in the chloride transport biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

transepithelial chloride transport Gene Set

From GO Biological Process Annotations

genes participating in the transepithelial chloride transport biological process from the curated GO Biological Process Annotations dataset.

cellular chloride ion homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the cellular chloride ion homeostasis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of intracellular calcium activated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of intracellular calcium activated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

chloride ion homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the chloride ion homeostasis biological process from the curated GO Biological Process Annotations dataset.

regulation of voltage-gated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of chloride transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of chloride transport biological process from the curated GO Biological Process Annotations dataset.

chloride channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the chloride channel complex cellular component from the curated GO Cellular Component Annotations dataset.

intracellular calcium activated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular calcium activated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-binding and phosphorylation-dependent chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-binding and phosphorylation-dependent chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium:chloride symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium:chloride symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

potassium:chloride symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium:chloride symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular-glycine-gated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular-glycine-gated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

volume-sensitive chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the volume-sensitive chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium:potassium:chloride symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium:potassium:chloride symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride ion binding Gene Set

From GO Molecular Function Annotations

genes performing the chloride ion binding molecular function from the curated GO Molecular Function Annotations dataset.

cation:chloride symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cation:chloride symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

gaba-gated chloride ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the gaba-gated chloride ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride-transporting atpase activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride-transporting atpase activity molecular function from the curated GO Molecular Function Annotations dataset.

2-(S-Glutathionyl)acetyl chloride Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 2-(S-Glutathionyl)acetyl chloride metabolite from the curated HMDB Metabolites of Enzymes dataset.

Doxacurium chloride Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Doxacurium chloride metabolite from the curated HMDB Metabolites of Enzymes dataset.

Chloroacetyl chloride Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Chloroacetyl chloride metabolite from the curated HMDB Metabolites of Enzymes dataset.

positive ferric chloride test Gene Set

From HPO Gene-Disease Associations

genes associated with the positive ferric chloride test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine chloride concentration Gene Set

From HPO Gene-Disease Associations

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

abnormality of chloride homeostasis Gene Set

From HPO Gene-Disease Associations

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

impaired reabsorption of chloride Gene Set

From HPO Gene-Disease Associations

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

Chloride channel, voltage gated Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel, voltage gated protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Intracellular chloride channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Intracellular chloride channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel, core Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel, core protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-K Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-K protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel calcium-activated Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel calcium-activated protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium-activated chloride channel protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium-activated chloride channel protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel CLIC-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel CLIC-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

decreased circulating chloride level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased urine chloride ion level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased urine chloride ion level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased urine chloride ion level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased urine chloride ion level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal chloride level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urine chloride ion level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine chloride ion level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased circulating chloride level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating chloride level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

diarrhea 1, secretory chloride, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the diarrhea 1, secretory chloride, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

chloride Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Cation-coupled Chloride cotransporters Gene Set

From Reactome Pathways

proteins participating in the Cation-coupled Chloride cotransporters pathway from the Reactome Pathways dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype 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.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy, cystic, without megalencephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cognitive impairment with or without cerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, without vestibular involvement, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary malformation without arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation 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.

Acrodysostosis 2, with or without hormone resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency 26 with or without neurologic abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 26 with or without neurologic abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

H2AX complex, isolated from cells without IR exposure Gene Set

From CORUM Protein Complexes

proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine without Aura from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE 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.

MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

Metaphyseal Dysplasia without Hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

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.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

Nonmedullary thyroid carcinoma, with or without cell oxyphilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nonmedullary thyroid carcinoma, with or without cell oxyphilia from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Migraine without Aura in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

migraine without aura Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

salmeterol with or without fluticasone propionate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease salmeterol with or without fluticasone propionate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate; cleft palate, isolated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lipor without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lipor without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with and without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with and without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies; cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

without Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term without in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cell cycle comprising mitosis without cytokinesis Gene Set

From GO Biological Process Annotations

genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations dataset.

Migraine without aura Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the migraine without aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

focal seizures without impairment of consciousness or awareness Gene Set

From HPO Gene-Disease Associations

genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

migraine without aura Gene Set

From HPO Gene-Disease Associations

genes associated with the migraine without aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Migraine without Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 15 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 15 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

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

paragangliomas 1, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the paragangliomas 1, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 14 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 14 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cognitive impairment with or without cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 3 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 3 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine without aura, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 8 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 8 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 5 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 5 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

?microtia with or without hearing impairment (ad) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 18 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 18 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

?testicular anomalies with or without congenital heart disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.

dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set

From OMIM Gene-Disease Associations

genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 2 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 2 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 1, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 20 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 20 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary hypertension, familial primary, 1, with or without hht Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 4 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 4 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, frontotemporal, with or without parkinsonism Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 9 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 9 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine without aura, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 1, with or without orofacial cleft Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.

{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 6 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 6 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract, pulverulent or cerulean, with or without microcornea Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set

From OMIM Gene-Disease Associations

genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

gyrate atrophy of choroid and retina with or without ornithinemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

adult i phenotype without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy, cystic, without megalencephaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

branchiootorenal syndrome 1, with or without cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

mcleod syndrome with or without chronic granulomatous disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the mcleod syndrome with or without chronic granulomatous disease phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 16 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 16 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

bifid nose with or without anorectal and renal anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

androgen insensitivity, partial, with or without breast cancer Gene Set

From OMIM Gene-Disease Associations

genes associated with the androgen insensitivity, partial, with or without breast cancer phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, progressive, with or without lipodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 16, with or without neurologic abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 16, with or without neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine with or without aura, susceptibility to Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine with or without aura, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 2, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperproinsulinemia, familial, with or without diabetes Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 7 without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 7 without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

anterior segment anomalies with or without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiac conduction disease with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 10, with or without ftd Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated OMIM Gene-Disease Associations dataset.