multiple small medullary renal cysts

Clear Filter

Results for "multiple small medullary renal cysts": 1002 gene sets

Name
multiple small medullary renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Small Medullary Renal Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Small Medullary Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
multiple renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Renal Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple renal cysts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple renal cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Medullary Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Medullary Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
carcinoma, medullary; lymphatic metastasis; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; lymphatic metastasis; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma, oxyphilic; carcinoma, medullary; carcinoma, papillary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma, oxyphilic; carcinoma, medullary; carcinoma, papillary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple glomerular cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple glomerular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Lung Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lung Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Glomerular Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Glomerular Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Renal cysts and diabetes syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.
renal corticomedullary cysts Gene Set From HPO Gene-Disease Associations genes associated with the renal corticomedullary cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical cysts Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal glomerulus cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal cysts and diabetes syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the renal cysts and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Renal Corticomedullary Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Corticomedullary Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cysts And Diabetes Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Cysts And Diabetes Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cortical Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Cortical Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Renal cysts and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cysts and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal cortical cysts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cortical cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
small inner medullary pyramid Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small inner medullary pyramid Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Renal Medullary Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Medullary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
SMARCB1-deficient renal medullary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SMARCB1-deficient renal medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Multiple synapse bouton, contacting multiple dendrites Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton, contacting multiple dendrites cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
multiple small vertebral fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d[<small>Dsmall>-Phe²]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Phe²]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[His⁵ <small>Dsmall>-Tyr⁶]GnRH Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [His⁵ <small>Dsmall>-Tyr⁶]GnRH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d[<small>Dsmall>-Pal²]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Pal²]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
<small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the <small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' protein domain from the InterPro Predicted Protein Domain Annotations dataset.
non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone Cysts, Aneurysmal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Cysts, Aneurysmal from the curated CTD Gene-Disease Associations dataset.
Cysts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cysts from the curated CTD Gene-Disease Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Megalencephalic leukoencephalopathy with subcortical cysts from the curated CTD Gene-Disease Associations dataset.
Ovarian Cysts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ovarian Cysts from the curated CTD Gene-Disease Associations dataset.
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.
cysts; epilepsy; tuberous sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cysts; epilepsy; tuberous sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts Gene Set From GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asymptomatic diseases; cyst; cysts; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease asymptomatic diseases; cyst; cysts; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cysts; pneumothorax; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cysts; pneumothorax; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cysts Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cysts in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
pancreatic cysts Gene Set From HPO Gene-Disease Associations genes associated with the pancreatic cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subependymal cysts Gene Set From HPO Gene-Disease Associations genes associated with the subependymal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
periventricular cysts Gene Set From HPO Gene-Disease Associations genes associated with the periventricular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hepatic cysts Gene Set From HPO Gene-Disease Associations genes associated with the hepatic cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
basal ganglia cysts Gene Set From HPO Gene-Disease Associations genes associated with the basal ganglia cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ovarian Cysts Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ovarian Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cysts Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Odontogenic Cysts Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Odontogenic Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
kidney medulla cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney medulla cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterus cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inner ear cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inner ear cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney corticomedullary cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney corticomedullary cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
gastric cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the gastric cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
urinary bladder cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the urinary bladder cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrium cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrium cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
prostate gland cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prostate gland cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lung cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lung cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cortex cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cortex cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epithelioid cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epithelioid cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ovary cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dermal cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dermal cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2a Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
aneurysmal bone cysts Gene Set From OMIM Gene-Disease Associations genes associated with the aneurysmal bone cysts phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebroretinal microangiopathy with calcifications and cysts Gene Set From OMIM Gene-Disease Associations genes associated with the cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 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.
Bone Cysts, Aneurysmal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bone Cysts, Aneurysmal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arachnoid Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arachnoid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Basal Ganglia Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Basal Ganglia Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bone Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bone Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Odontogenic Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Odontogenic Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rathke Cleft Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rathke Cleft Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intracranial Arachnoid Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Arachnoid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subchondral Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subchondral Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jaw Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jaw Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pilar And Trichilemmal Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pilar And Trichilemmal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colloid Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Colloid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periventricular Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periventricular Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subependymal Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subependymal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Interhemispheric Cysts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Interhemispheric Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Megalencephalic leukoencephalopathy with subcortical cysts from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Blessig's cysts Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blessig's cysts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megalencephalic leukoencephalopathy with subcortical cysts 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancreatic cysts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancreatic cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatic cysts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Periventricular cysts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periventricular cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
central medullary reticular group, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral medullary reticular group, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
lateral medullary reticular group, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central medullary reticular group, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
medullary hindbrain (medulla) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in medullary hindbrain (medulla) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Medullary reticular nucleus, dorsal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Medullary reticular nucleus, ventral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Medullary reticular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Histiocytic medullary reticulosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Histiocytic medullary reticulosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Medullary cystic kidney disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lateral Medullary Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lateral Medullary Syndrome from the curated CTD Gene-Disease Associations dataset.
Thyroid cancer, medullary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid cancer, medullary from the curated CTD Gene-Disease Associations dataset.
Familial medullary thyroid carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.
Medullary Cystic Kidney Disease 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset.
Carcinoma, Medullary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Medullary from the curated CTD Gene-Disease Associations dataset.
Medullary cystic kidney disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medullary cystic kidney disease 1 from the curated CTD Gene-Disease Associations dataset.
breast medullary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
thyroid medullary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thyroid medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lateral medullary syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lateral medullary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary medullary thyroid carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary medullary thyroid carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thyroid cancer; thyroid carcinoma, sporadic medullary Gene Set From GAD Gene-Disease Associations genes associated with the disease thyroid cancer; thyroid carcinoma, sporadic medullary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; carcinoma, papillary; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; carcinoma, papillary; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
medullary sponge kidney disease Gene Set From GAD Gene-Disease Associations genes associated with the disease medullary sponge kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; neoplasm metastasis; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; neoplasm metastasis; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; hyperplasia; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; hyperplasia; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; neoplasm recurrence, local; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; neoplasm recurrence, local; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
medullary Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term medullary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
outer medullary collecting duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
inner medullary collecting duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
medullary reticular formation development Gene Set From GO Biological Process Annotations 2015 genes participating in the medullary reticular formation development biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormality of the medullary cavity of the long bones Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
medullary thyroid carcinoma Gene Set From HPO Gene-Disease Associations genes associated with the medullary thyroid carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stenosis of the medullary cavity of the long bones Gene Set From HPO Gene-Disease Associations genes associated with the stenosis of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenal medullary hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Carcinoma, Medullary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Medullary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neoplasms, Ductal, Lobular, and Medullary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Ductal, Lobular, and Medullary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
dilated lymph node medullary sinus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated lymph node medullary sinus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymph node medullary sinus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node medullary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hair medullary septa cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lymph node medullary cord hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lymph node medullary cord hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal kidney medullary ray morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney medullary ray morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymph node medullary cord morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node medullary cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene Set From OMIM Gene-Disease Associations genes associated with the diaphyseal medullary stenosis with malignant fibrous histiocytoma phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary thyroid carcinoma Gene Set From OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary thyroid carcinoma, familial Gene Set From OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary cystic kidney disease 2 Gene Set From OMIM Gene-Disease Associations genes associated with the medullary cystic kidney disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary cystic kidney disease 1 Gene Set From OMIM Gene-Disease Associations genes associated with the medullary cystic kidney disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
inner medullary collecting duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
thymic medullary epithelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thymic medullary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary thyroid carcinoma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary thyroid carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary carcinoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary thyroid carcinoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary thyroid carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary collecting duct cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
inner medullary collecting duct cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
thymic medullary epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thymic medullary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary collecting duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
medullary thyroid carcinoma Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease medullary thyroid carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Thymus-medullary thymic epithelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Thymus-medullary thymic epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Medullary Carcinoma With Lymphoid Stroma Of Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Carcinoma With Lymphoid Stroma Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Neoplasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Neoplasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Non-Medullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Medullary Thyroid Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Medullary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Sponge Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Sponge Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Medullary Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Medullary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Carcinoma, Sporadic Medullary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Carcinoma, Sporadic Medullary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Medullary-Follicular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Medullary-Follicular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Nephrocalcinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Nephrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lateral Medullary Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lateral Medullary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Sponge Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Sponge Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Cystic Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Cystic Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Cystic Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Cystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diaphyseal Medullary Stenosis With Bone Malignancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Bone Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Medullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Medullary Cavity Of The Long Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Medullary Cavity Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Expanded Metacarpals With Widened Medullary Cavities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Metacarpals With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Expanded Metatarsals With Widened Medullary Cavities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Metatarsals With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Expanded Phalanges With Widened Medullary Cavities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Phalanges With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adrenal Medullary Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adrenal Medullary Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Narrowing Of Medullary Canal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrowing Of Medullary Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
outer medullary collecting duct development Gene Set From GO Biological Process Annotations 2023 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset.
inner medullary collecting duct development Gene Set From GO Biological Process Annotations 2023 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal lymph node medullary cord morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph node medullary cord morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lymph node medullary cord hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node medullary cord hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hair medullary septa cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal kidney medullary ray morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney medullary ray morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dilated lymph node medullary sinus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated lymph node medullary sinus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Kidney - L2 - Inner Medullary Collecting Duct Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Medullary Fibroblast Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Medullary Fibroblast cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Medullary Thick Ascending Limb Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Outer Medullary Collecting Duct Principal Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Inner Medullary Collecting Duct Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Medullary Fibroblast Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Medullary Fibroblast cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Medullary Thick Ascending Limb Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Outer Medullary Collecting Duct Principal Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Medullary cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medullary cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Interstitial Cell (Medullary)_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Interstitial Cell (Medullary)_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Inner Medullary Collecting Ductal cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Inner Medullary Collecting Ductal cell_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Medullary thymus epithelial cell_Thymus_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medullary thymus epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mature medullary thymic epithelial cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Mature medullary thymic epithelial cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Immature medullary thymic epithelial cell_Thymus_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Immature medullary thymic epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Medullary cell_Thymus_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medullary cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Medullary reticular cell (MedRCs)_Undefined_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medullary reticular cell (MedRCs)_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset.
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset.
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B dataset.
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B dataset.
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B dataset.
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
outer medullary collecting duct development Gene Set From GO Biological Process Annotations 2025 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset.
inner medullary collecting duct development Gene Set From GO Biological Process Annotations 2025 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset.
Thyroid gland medullary carcinoma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thyroid gland medullary carcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Thyroid gland medullary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thyroid gland medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Breast medullary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lateral medullary syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lateral medullary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Medullary colon carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medullary colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diaphyseal medullary stenosis with malignant fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thymic medullary epithelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thymic medullary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Thymic medullary epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thymic medullary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary collecting duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Inner medullary collecting duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary thyroid carcinoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary thyroid carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary carcinoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Inner medullary collecting duct cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary thyroid carcinoma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary thyroid carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary collecting duct cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Medullary breast carcinoma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary breast carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Histiocytic medullary reticulosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Histiocytic medullary reticulosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant medullary cystic kidney disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant medullary cystic kidney disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Invasive medullary breast carcinoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Invasive medullary breast carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diaphyseal medullary stenosis-bone malignancy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diaphyseal medullary stenosis-bone malignancy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
diabetes, post-renal transplant; post-renal transplant diabetes Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, post-renal transplant; post-renal transplant diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal involvement and renal sequelae Gene Set From GAD Gene-Disease Associations genes associated with the disease renal involvement and renal sequelae in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set From Biocarta Pathways proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.
CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Multiple synostoses syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 15, multiple types Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant, multiple types, with microcornea Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple fibrofolliculomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple fibrofolliculomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple sulfatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple pterygium syndrome Escobar type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple gastrointestinal atresias Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple exostoses type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple fibroadenomas of the breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple fibroadenomas of the breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOMATOSIS, MULTIPLE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LIPOMATOSIS, MULTIPLE from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.
Cafe au lait spots, multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cafe au lait spots, multiple from the curated CTD Gene-Disease Associations dataset.
Multiple Organ Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Organ Failure from the curated CTD Gene-Disease Associations dataset.
EXOSTOSES, MULTIPLE, TYPE II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE II from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 2a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Multiple Myeloma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Myeloma from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.
Multiple Synostoses Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Synostoses Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
CATARACT 32, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Exostoses, Multiple Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset.
Hamartoma Syndrome, Multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
CATARACT 6, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia from the curated CTD Gene-Disease Associations dataset.
Exostoses, Multiple, Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple, Type III from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis from the curated CTD Gene-Disease Associations dataset.
Multiple Chemical Sensitivity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Chemical Sensitivity from the curated CTD Gene-Disease Associations dataset.
Multiple synostoses syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple synostoses syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis, Relapsing-Remitting from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 2b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2b from the curated CTD Gene-Disease Associations dataset.
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant, Multiple Types 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Multiple pterygium syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple pterygium syndrome from the curated CTD Gene-Disease Associations dataset.
Abnormalities, Multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Abnormalities, Multiple from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia, Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia, Type IV from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.
CATARACT 3, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.
EXOSTOSES, MULTIPLE, TYPE I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE I from the curated CTD Gene-Disease Associations dataset.
CATARACT 4, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
MULTIPLE SYNOSTOSES SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE SYNOSTOSES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Multiple Sclerosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Multiple Myeloma Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Multiple Myeloma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hereditary multiple exostoses Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple sclerosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple carboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple myeloma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple sclerosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
multiple intestinal atresia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple myeloma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary multiple exostoses Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple mucosal neuroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple chemical sensitivity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple symmetrical lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetrical lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple carboxylase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple symmetric lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
relapsing-remitting multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set From GAD Gene-Disease Associations genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; optic neuritis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; shock, septic; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burns; multiple organ failure; shock Gene Set From GAD Gene-Disease Associations genes associated with the disease burns; multiple organ failure; shock in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis (age of onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; diabetes, type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; multiple sclerosis; hiv Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; multiple sclerosis; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
susceptibility to multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease susceptibility to multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic predisposition to disease; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hamartoma syndrome, multiple Gene Set From GAD Gene-Disease Associations genes associated with the disease hamartoma syndrome, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaw diseases; multiple myeloma; osteonecrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease jaw diseases; multiple myeloma; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis(ppmultiple sclerosis) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis(ppmultiple sclerosis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
encephalomyelitis, autoimmune, experimental; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease encephalomyelitis, autoimmune, experimental; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple autoimmune diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; neuromyelitis optica Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; neuromyelitis optica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; plasmacytoma Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; plasmacytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normalized brain volume, multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, systemic; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple chemical sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; pneumonia; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; short bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; iga nephropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
churg-strauss syndrome; multiple sclerosis; wegener granulomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease churg-strauss syndrome; multiple sclerosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tic; combined vocal and multiple motor; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2b Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2a Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; multiple myeloma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloma, multiple Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloma, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c, chronic; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis (severity) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (severity) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple oesophageal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epstein-barr virus infections; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease epstein-barr virus infections; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary multiple exostoses Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary multiple exostoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; pneumonia; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone diseases; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of multiple sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft vs host disease; leukemia; multiple myeloma; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graft vs host disease; leukemia; multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; neoplasm recurrence, local Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; carcinoma; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term multiple in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Multiple sclerosis--Brain Glutamate Levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis or amyotrophic lateral sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma (IgH translocation) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (severity) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma (hyperdiploidy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (OCB status) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
multiple myeloma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
multiple sclerosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
multiple mitochondrial dna deletions Gene Set From GWASdb SNP-Phenotype Associations genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
multiple myeloma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the multiple myeloma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
multiple exostoses Gene Set From HPO Gene-Disease Associations genes associated with the multiple exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple gastric polyps Gene Set From HPO Gene-Disease Associations genes associated with the multiple gastric polyps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple cutaneous leiomyomas Gene Set From HPO Gene-Disease Associations genes associated with the multiple cutaneous leiomyomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple impacted teeth Gene Set From HPO Gene-Disease Associations genes associated with the multiple impacted teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple enchondromatosis Gene Set From HPO Gene-Disease Associations genes associated with the multiple enchondromatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple prenatal fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple joint contractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple joint contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple rows of eyelashes Gene Set From HPO Gene-Disease Associations genes associated with the multiple rows of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple myeloma Gene Set From HPO Gene-Disease Associations genes associated with the multiple myeloma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple plantar creases Gene Set From HPO Gene-Disease Associations genes associated with the multiple plantar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular preexcitation with multiple accessory pathways Gene Set From HPO Gene-Disease Associations genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple digital exostoses Gene Set From HPO Gene-Disease Associations genes associated with the multiple digital exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bowing of limbs due to multiple fractures Gene Set From HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple suture craniosynostosis Gene Set From HPO Gene-Disease Associations genes associated with the multiple suture craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple lipomas Gene Set From HPO Gene-Disease Associations genes associated with the multiple lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of multiple cell lineages in the bone marrow Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple carpal ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple mitochondrial dna deletions Gene Set From HPO Gene-Disease Associations genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple pterygia Gene Set From HPO Gene-Disease Associations genes associated with the multiple pterygia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple cafe-au-lait spots Gene Set From HPO Gene-Disease Associations genes associated with the multiple cafe-au-lait spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the multiple palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple rib fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple rib fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple lentigines Gene Set From HPO Gene-Disease Associations genes associated with the multiple lentigines phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple skeletal anomalies Gene Set From HPO Gene-Disease Associations genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Trauma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Trauma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Organ Failure Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Organ Failure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 2b Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2b phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 2a Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2a phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Myeloma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Myeloma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Relapsing-Remitting phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Exostoses, Multiple Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Exostoses, Multiple Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Abnormalities, Multiple Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Abnormalities, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hamartoma Syndrome, Multiple Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hamartoma Syndrome, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 1 Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Chemical Sensitivity Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Chemical Sensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neoplasms, Multiple Primary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Multiple Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
multiple major aortopulmonary collateral arteries Gene Set From MPO Gene-Phenotype Associations gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intestinal atresia, multiple Gene Set From OMIM Gene-Disease Associations genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.
?epiphyseal dysplasia, multiple, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 5, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
adenomas, multiple colorectal Gene Set From OMIM Gene-Disease Associations genes associated with the adenomas, multiple colorectal phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 9, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia iib Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iib phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia iia Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iia phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple pterygium syndrome, lethal type Gene Set From OMIM Gene-Disease Associations genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 3, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple myeloma, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple myeloma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 1, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple system atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
orolaryngeal cancer, multiple, Gene Set From OMIM Gene-Disease Associations genes associated with the orolaryngeal cancer, multiple, phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple fibroadenomas of the breast Gene Set From OMIM Gene-Disease Associations genes associated with the multiple fibroadenomas of the breast phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitiligo-associated multiple autoimmune disease susceptiblity 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptiblity 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 20, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set From OMIM Gene-Disease Associations genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple mitochondrial dysfunctions syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple mitochondrial dysfunctions syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital heart defects, multiple types, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital heart defects, multiple types, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 14, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
venous malformations, multiple cutaneous and mucosal Gene Set From OMIM Gene-Disease Associations genes associated with the venous malformations, multiple cutaneous and mucosal phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 12, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 39, multiple types, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopia and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness 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.
multiple endocrine neoplasia, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitiligo-associated multiple autoimmune disease susceptibility 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 34, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 6, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 2, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple myeloma, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple myeloma, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 16, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 15, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple sulfatase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the multiple sulfatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple synostoses syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple synostoses syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple synostoses syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple synostoses syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 17, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 4, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 31, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 10, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple mitochondrial dysfunctions syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple self-healing squamous epithelioma, susceptiblity to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple self-healing squamous epithelioma, susceptiblity to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set From Reactome Pathways 2014 proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways dataset.
Defective HLCS causes multiple carboxylase deficiency Gene Set From Reactome Pathways 2014 proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.
multiple myeloma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
multiple myeloma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Multiple Chronic Conditions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Chronic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Relapsing-Remitting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lipomatosis, Multiple Symmetrical Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lipomatosis, Multiple Symmetrical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitiligo-Associated Multiple Autoimmune Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitiligo-Associated Multiple Autoimmune Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lipomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lipomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Adenomatous Polyps Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Endocrine Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Multiple Exostoses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Epiphyseal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Epiphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Gastrointestinal Atresias (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Gastrointestinal Atresias (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichoepitheliomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Primary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Polyps Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meningiomas, Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meningiomas, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Myeloma Progression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma Progression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lacunar Infarcts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lacunar Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Multiple Mole-Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Acute Fulminating Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Fulminating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Acute Relapsing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Relapsing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis In Children Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Opticospinal Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Opticospinal Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sulfatase Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Carboxylase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Carboxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Joint Dislocations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis Relapse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis Relapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Mitochondrial Dysfunctions Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Mitochondrial Dysfunctions Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lentigines Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lentigines in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Nevi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Nevi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Fibrofolliculomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Fibrofolliculomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymptomatic Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Self-Healing Squamous Epithelioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Self-Healing Squamous Epithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Biliary Hamartomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Biliary Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome, Lethal Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Linear Skin Defects With Multiple Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Linear Skin Defects With Multiple Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Factor Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Abscesses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Abscesses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Lipomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Trichoepitheliomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Trichoepitheliomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Synostoses Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Synostoses Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Allergies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Allergies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Neoplasm Of Lung - Multiple Primary Sites Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Lung - Multiple Primary Sites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Basal Cell Papillomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Basal Cell Papillomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exostoses, Multiple, Type Ii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exostoses, Multiple, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Multiple Osteochondromas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Osteochondromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Osteochondroma Of Long Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Osteochondroma Of Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Evanescent White Dot Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Evanescent White Dot Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichodiscomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Multiple Cell Lineages In The Bone Marrow Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Multiple Cell Lineages In The Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevi Flammei, Familial Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Non-Ossifying Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Non-Ossifying Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Hemangioblastomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Hemangioblastomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Milia, Multiple Eruptive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Milia, Multiple Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pancreatic Beta-Cell Adenomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pancreatic Beta-Cell Adenomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indolent Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indolent Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Neuropathies, Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Neuropathies, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Fibroadenomas Of The Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Fibroadenomas Of The Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Digital Exostoses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Digital Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lentigines/Leopard Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lentigines/Leopard Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lineage Myelodysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lineage Myelodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Cranial Nerve Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cranial Nerve Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Aneurysms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Aneurysms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple, Subcutaneous Nodules Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple, Subcutaneous Nodules in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous And Mucosal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Venous Malformations, Multiple Cutaneous And Mucosal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis Lesion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Self-Healing Epithelioma Of Ferguson-Smith Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Self-Healing Epithelioma Of Ferguson-Smith in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Ventricular Septal Defects Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Ventricular Septal Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Tumors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Tumors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Prenatal Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Prenatal Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Malignancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Organ Failure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Organ Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Unerupted Teeth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Unerupted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Suture Craniosynostosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Suture Craniosynostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Skeletal Anomalies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Skeletal Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Palmar Creases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Palmar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Plantar Creases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Plantar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Joint Dislocations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Chemical Sensitivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Chemical Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Myeloma, T(11;14) Type, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Myeloma, T(11;14) Type, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Impacted Teeth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Impacted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cancer Of Multiple Types, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cancer Of Multiple Types, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Pterygia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Pterygia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Contractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Carpal Ossification Centers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Carpal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bowing Of Limbs Due To Multiple Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of Limbs Due To Multiple Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Long-Bone Exostoses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Long-Bone Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Dysmorphism With Multiple Malformations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Dysmorphism With Multiple Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neoplasms, Multiple Primary Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neoplasms, Multiple Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Multiple Nuclear Dots Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Multiple Nuclear Dots Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Mitochondrial Dna Deletions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Preexcitation With Multiple Accessory Pathways Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Preexcitation With Multiple Accessory Pathways in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Self-Healing Squamous Epithelioma, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Self-Healing Squamous Epithelioma, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Rows Of Eyelashes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Rows Of Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
multiple spine synapse organization, single dendrite Gene Set From GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2023 dataset.
multiple spine synapse organization Gene Set From GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2023 dataset.
CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
multiple major aortopulmonary collateral arteries Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
multiple persisting craniopharyngeal ducts Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the multiple persisting craniopharyngeal ducts phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Multiple pluripotent progenitor cell_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Multiple pluripotent progenitor cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Multiple myeloma(MM) cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Multiple myeloma(MM) cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Multiple ductal cell_Pancreatic duct_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Multiple ductal cell_Pancreatic duct_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Multiple epiphyseal dysplasia and pseudoachondroplasia genes Gene Set From WikiPathways Pathways 2024 proteins participating in the Multiple epiphyseal dysplasia and pseudoachondroplasia genes pathway from the WikiPathways Pathways 2024 dataset.
Defective HLCS causes multiple carboxylase deficiency Gene Set From Reactome Pathways 2024 proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways 2024 dataset.
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models Gene Set From Reactome Pathways 2024 proteins participating in the Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models pathway from the Reactome Pathways 2024 dataset.
Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set From Reactome Pathways 2024 proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways 2024 dataset.
multiple spine synapse organization, single dendrite Gene Set From GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2025 dataset.
multiple spine synapse organization Gene Set From GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2025 dataset.
Multiple endocrine neoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple endocrine neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple endocrine neoplasia type 2A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple endocrine neoplasia type 2A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary multiple exostoses Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary multiple exostoses from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple myeloma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple myeloma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Noonan syndrome with multiple lentigines Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Noonan syndrome with multiple lentigines from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple mitochondrial dysfunctions syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple carboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple sclerosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple sclerosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple acyl-CoA dehydrogenase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple cutaneous and mucosal venous malformations Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple cutaneous and mucosal venous malformations from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Linear skin defects with multiple congenital anomalies 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Linear skin defects with multiple congenital anomalies 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple myeloma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple myeloma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple synostoses syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple acyl-CoA dehydrogenase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary multiple exostoses Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
relapsing-remitting multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple endocrine neoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple endocrine neoplasia type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple intestinal atresia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple carboxylase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary arterial and articular multiple calcification syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary arterial and articular multiple calcification syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple endocrine neoplasia type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple synostoses syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 9 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 9 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome with multiple lentigines Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple synostoses syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial multiple lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial multiple lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple symmetric lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple chemical sensitivity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple endocrine neoplasia type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive relapsing multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 8 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 8 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Linear skin defects with multiple congenital anomalies 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 6 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 6 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple synostoses syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial multiple nevi flammei Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial multiple nevi flammei in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple endocrine neoplasia type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple cutaneous and mucosal venous malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple cutaneous and mucosal venous malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 1 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 1 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome with multiple lentigines 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 32 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 32 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome with multiple lentigines 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple benign circumferential skin creases on limbs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 4 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 4 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 11 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 11 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 10 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 10 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 3 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 3 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 21 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 21 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mucosal neuroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 31 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 31 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 14 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 14 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 34 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 34 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Linear skin defects with multiple congenital anomalies 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Linear skin defects with multiple congenital anomalies 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome with multiple lentigines 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia with myopia and deafness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia with myopia and deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple myeloma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Multiple myeloma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Multiple synapse bouton Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Multiple synapse bouton, contacting single dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton, contacting single dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple symmetric lipomatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple symmetric lipomatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple acyl-CoA dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple sulfatase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple epiphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vitiligo-associated multiple autoimmune disease susceptibility Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitiligo-associated multiple autoimmune disease susceptibility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial multiple trichoepitheliomata Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple trichoepitheliomata phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 12 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 12 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple myeloma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple myeloma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple synostoses syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple synostoses syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 1 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 1 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple cutaneous and mucosal venous malformations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple cutaneous and mucosal venous malformations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple sclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple self-healing squamous epithelioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple self-healing squamous epithelioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MULTIPLE MYEL Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE MYEL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple endocrine neoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple endocrine neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MULTIPLE ENDOCRINE NEOPLA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE ENDOCRINE NEOPLA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 4 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 4 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 3 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 3 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 9 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 9 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary arterial and articular multiple calcification syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary arterial and articular multiple calcification syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MULTIPLE JOINT DISLOCATI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE JOINT DISLOCATI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple joint dislocations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple mitochondrial dysfunctions syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple mitochondrial dysfunctions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 16 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 16 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 39 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 39 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KAT6B-related multiple congenital anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KAT6B-related multiple congenital anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple gastrointestinal atresias Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial multiple nevi flammei Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple nevi flammei phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 14 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 14 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 15 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 15 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 10 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 10 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple benign circumferential skin creases on limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal multiple mitochondrial dysfunctions syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal multiple mitochondrial dysfunctions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 34 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 34 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 11 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 11 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 6 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 6 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 5 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 5 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 21 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 21 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 22 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 22 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies/dysmorphic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies/dysmorphic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary Multiple Osteochondromatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary Multiple Osteochondromatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 19 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 19 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 17 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 17 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe dermatitis-multiple allergies-metabolic wasting syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe dermatitis-multiple allergies-metabolic wasting syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive multiple sclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple joint contractures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint contractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple mitochondrial dysfunctions syndrome 9b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple mitochondrial dysfunctions syndrome 9b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 20 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 20 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 31 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 31 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-neurodevelopmental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple fibroadenoma of the breast Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple fibroadenoma of the breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple myeloma (survival) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to interferon beta in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to interferon beta in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple myeloma and monoclonal gammopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma and monoclonal gammopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy (pathologically confirmed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy (pathologically confirmed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
B-cell malignancies (chronic lymphocytic leukemia, Hodgkin lymphoma or multiple myeloma) (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the B-cell malignancies (chronic lymphocytic leukemia, Hodgkin lymphoma or multiple myeloma) (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Decreased low contrast letter acuity in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Decreased low contrast letter acuity in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Drug-induced liver injury in interferon-beta-treated multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Drug-induced liver injury in interferon-beta-treated multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depression in multiple sclerosis (pre-diagnosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (pre-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depression in multiple sclerosis (post-diagnosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (post-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depression in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relapse in treatment-naive multiple sclerosis (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relapse in treatment-naive multiple sclerosis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis or amyotrophic lateral sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Oligoclonal band status in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Oligoclonal band status in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Immunoglobulin G index levels in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin G index levels in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Uterine fibroid number (single vs multiple) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uterine fibroid number (single vs multiple) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis (severity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis--Brain Glutamate Levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis (OCB status) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple myeloma (IgH translocation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Clostridium difficile infection in multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Clostridium difficile infection in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relapse in multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relapse in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and systolic blood pressure (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and systolic blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and body mass index (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and body mass index (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and waist-to-hip-ratio (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and waist-to-hip-ratio (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and type 2 diabetes (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and type 2 diabetes (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and C-reactive protein levels (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and C-reactive protein levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and triglyceride levels (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and triglyceride levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and LDL levels (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and LDL levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis and HDL levels (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and HDL levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple keratinocyte cancers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple keratinocyte cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic lymphocytic leukemia or multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic lymphocytic leukemia or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diffuse large B-cell lymphoma or multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diffuse large B-cell lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Follicular lymphoma or multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Follicular lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Marginal zone lymphoma or multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippo signaling pathway - multiple species Gene Set From KEGG Pathways 2026 proteins participating in the Hippo signaling pathway - multiple species pathway from the KEGG Pathways 2026 dataset.
Apoptosis - multiple species Gene Set From KEGG Pathways 2026 proteins participating in the Apoptosis - multiple species pathway from the KEGG Pathways 2026 dataset.
Longevity regulating pathway - multiple species Gene Set From KEGG Pathways 2026 proteins participating in the Longevity regulating pathway - multiple species pathway from the KEGG Pathways 2026 dataset.
Pathways of neurodegeneration - multiple diseases Gene Set From KEGG Pathways 2026 proteins participating in the Pathways of neurodegeneration - multiple diseases pathway from the KEGG Pathways 2026 dataset.
Non-small cell lung cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brain small vessel disease with hemorrhage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
mitochondrial small ribosomal subunit Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
preribosome, small subunit precursor Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, small subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small nuclear ribonucleoprotein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nuclear ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
small nucleolar ribonucleoprotein complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

Harmonizome 3.0

multiple small medullary renal cysts Gene Set

Multiple Small Medullary Renal Cysts Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene Set

adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene Set

carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT Gene Set

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H Gene Set

multiple renal cysts Gene Set

Multiple Renal Cysts Gene Set

Multiple renal cysts Gene Set

Medullary Cysts Gene Set

carcinoma, medullary; lymphatic metastasis; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set

carcinoma, medullary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set

adenoma, oxyphilic; carcinoma, medullary; carcinoma, papillary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene Set

multiple glomerular cysts Gene Set

Multiple Lung Cysts Gene Set

Multiple Cysts Gene Set

Multiple Glomerular Cysts Gene Set

carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set

carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

Renal cysts and diabetes syndrome Gene Set

renal corticomedullary cysts Gene Set

renal cortical cysts Gene Set

renal glomerulus cysts Gene Set

renal cysts and diabetes syndrome Gene Set

Renal Corticomedullary Cysts Gene Set

Renal Cysts And Diabetes Syndrome Gene Set

Renal Cortical Cysts Gene Set

Renal cysts and diabetes syndrome Gene Set

Renal cortical cysts Gene Set

small inner medullary pyramid Gene Set

small inner medullary pyramid Gene Set

Renal Medullary Carcinoma Gene Set

SMARCB1-deficient renal medullary carcinoma Gene Set

chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene Set

chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene Set

chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene Set

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set

multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set

Multiple synapse bouton, contacting multiple dendrites Gene Set

multiple small vertebral fractures Gene Set

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

d[<small>Dsmall>-Phe2]AVP Gene Set

[125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

[Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP Gene Set

[<small>Dsmall>-Bpa5 Ile13]motilin (human) Gene Set

[tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP Gene Set

[His5 <small>Dsmall>-Tyr6]GnRH Gene Set

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP Gene Set

[<small>Lsmall>-Bpa5 Ile13]motilin (human) Gene Set

[des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

[Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP Gene Set

[Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin Gene Set

d[<small>Dsmall>-Pal2]AVP Gene Set

d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP Gene Set

[Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP Gene Set

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP Gene Set

[<small>Dsmall>-Lys1 des-Arg10]kallidin Gene Set

[125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

<small>Dsmall>-Lys0-[des-Arg10]kallidin Gene Set

[Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP Gene Set

[125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene Set

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

Megalencephalic leukoencephalopathy with subcortical cysts 2a Gene Set

Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene Set

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

Bone Cysts, Aneurysmal Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ <small>Dsmall>-Tic⁹]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO₂H Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷]OT Gene Set

[Mpa¹ <small>Dsmall>-Tyr(Et)² <small>Dsmall>-Tic⁷ Aib⁹]OT Gene Set

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO₂H Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d[<small>Dsmall>-Phe²]AVP Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

[Phaa¹ <small>Dsmall>-Tyr² Val⁴ Arg⁶ Arg-NH₂⁹]AVP Gene Set

[<small>Dsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set

[tBaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Arg-NH₂⁸ des-Gly⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂⁹]AVP Gene Set

[His⁵ <small>Dsmall>-Tyr⁶]GnRH Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴]AVP Gene Set

[<small>Lsmall>-Bpa⁵ Ile¹³]motilin (human) Gene Set

[des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Et)² Val⁴ Lys⁶ Tyr-NH₂⁸ des-Gly⁹]AVP Gene Set

[Sar <small>Dsmall>-Phe⁸ des-Arg⁹]bradykinin Gene Set

d[<small>Dsmall>-Pal²]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Val⁴ Tyr-NH₂⁹]AVP Gene Set

d(CH₂)₅[<small>Dsmall>-Ile² Ile⁴ Ala-NH₂]AVP Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Me)² Arg⁶ Tyr-NH₂⁹]AVP Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Tyr(Et)² Ile⁴ Tyr-NH₂⁹]AVP Gene Set

[<small>Dsmall>-Lys¹ des-Arg¹⁰]kallidin Gene Set

[¹²⁵I]d(CH₂)₅[<small>Dsmall>-Ile² Val⁴ Tyr-NH₂⁹]AVP Gene Set

<small>Dsmall>-Lys⁰-[des-Arg¹⁰]kallidin Gene Set

[Phaa¹ <small>Dsmall>-Tyr(Et)² Lys⁶ des-Gly⁹]AVP Gene Set

[¹²⁵I][des-Gly¹⁰ <small>Dsmall>-Ala⁶]GnRH N-ethylamide Gene Set