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High Risk Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Risk Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardioembolism (High-Risk/Medium-Risk) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardioembolism (High-Risk/Medium-Risk) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased risk to develop myelodysplastic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Increased risk to develop myelodysplastic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
high tnf levels is not a risk factor for venous thromboem Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high tnf levels is not a risk factor for venous thromboem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuroblastoma (high-risk) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuroblastoma (high-risk) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high coronary heart disease risk particularly affects ser Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high coronary heart disease risk particularly affects ser in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Neuroblastoma (high-risk) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Neuroblastoma (high-risk) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
High-Risk Neuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Risk Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Risk Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Risk Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Circulating leptin levels in high cardiovascular risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Circulating leptin levels in high cardiovascular risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Circulating leptin levels x sex interaction in high cardiovascular risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Circulating leptin levels x sex interaction in high cardiovascular risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 1 diabetes in high risk HLA genotype individuals (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 1 diabetes in high risk HLA genotype individuals (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 1 diabetes autoantibodies in high risk HLA genotype individuals (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 1 diabetes autoantibodies in high risk HLA genotype individuals (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cervical high-risk human papilloma virus infection (persistent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cervical high-risk human papilloma virus infection (persistent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cervical high-risk human papilloma virus infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cervical high-risk human papilloma virus infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
BRCA1/2-negative high-risk breast cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BRCA1/2-negative high-risk breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neuroblastoma (high-risk) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuroblastoma (high-risk) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
high plasma concentrations of high density lipoprotein ch Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high plasma concentrations of high density lipoprotein ch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
HIgh-sensitivity cardiac troponin T levels (high vs low) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIgh-sensitivity cardiac troponin T levels (high vs low) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene SetFrom 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. |
myelodysplastic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid; myelodysplastic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid; myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the myelodysplastic syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
myelodysplastic syndrome, preleukemic Gene SetFrom OMIM Gene-Disease Associations genes associated with the myelodysplastic syndrome, preleukemic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{myelodysplastic syndrome, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {myelodysplastic syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myelodysplastic syndrome, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the myelodysplastic syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
Adult Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Myeloid Leukemia With Multilineage Dysplasia Following Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Myeloid Leukemia With Multilineage Dysplasia Following Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Therapy-Related Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Therapy-Related Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Therapy-Related Acute Myeloid Leukemia And Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Therapy-Related Acute Myeloid Leukemia And Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypocellular Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypocellular Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myelodysplastic syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myelodysplastic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myelodysplastic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myelodysplastic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myelodysplastic syndrome progressed to acute myeloid leukemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myelodysplastic syndrome progressed to acute myeloid leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
cardiovascular risk; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular risk; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Myelodysplastic Syndromes Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myelodysplastic Syndromes from the curated CTD Gene-Disease Associations dataset. |
Myelodysplastic-Myeloproliferative Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myelodysplastic-Myeloproliferative Diseases from the curated CTD Gene-Disease Associations dataset. |
myelodysplastic myeloproliferative cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myelodysplastic myeloproliferative cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; leukemia, myelodysplastic (trlimds) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; leukemia, myelodysplastic (trlimds) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome breakage; dna damage; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome breakage; dna damage; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; myelodysplastic syndromes Gene SetFrom 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. |
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia 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 SetFrom 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. |
anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myelomonocytic, chronic; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndromes; parkinson disease; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; parkinson disease; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoproliferative disorders; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome deletion; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome deletion; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; myelodysplastic syndromes; preleukemia Gene SetFrom 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. |
chromosome aberrations; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myelodysplastic syndromes; myeloproliferative disorders; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; myeloproliferative disorders; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene SetFrom 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. |
myelodysplastic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term myelodysplastic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
MDS - Myelodysplastic syndrome_Bone marrow stem cell_GSE2779 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MDS - Myelodysplastic syndrome_Bone marrow stem cell_GSE2779 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
MDS - Myelodysplastic syndrome_Bone marrow stem cell_GSE4619 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MDS - Myelodysplastic syndrome_Bone marrow stem cell_GSE4619 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
myelodysplastic myeloproliferative cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease myelodysplastic myeloproliferative cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Myelodysplastic Syndromes Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Myelodysplastic Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
De Novo Myelodysplastic Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease De Novo Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Myelodysplastic Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
myelodysplastic/myeloproliferative neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myelodysplastic/myeloproliferative neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Non-del(5q) myelodysplastic syndromes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-del(5q) myelodysplastic syndromes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased chromosome aberrations and higher lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; insulin; cardiovascular disease risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; insulin; cardiovascular disease risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infectious risk and outcome in surgical intensive care patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infectious risk and outcome in surgical intensive care patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric carcinoma risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric carcinoma risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of osteoporotic fractures case control study Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of osteoporotic fractures case control study in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
financial and psychological risk attitudes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease financial and psychological risk attitudes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased risk of insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased risk of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetes; reduced prostate cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetes; reduced prostate cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; decreased cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; decreased cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary and sporadic prostate cancer risk. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary and sporadic prostate cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
circulating protein c levels and thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased fracture risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anthropometric and metabolic traits, relative to cardiovascular risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anthropometric and metabolic traits, relative to cardiovascular risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma protein c levels and thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease-reduced risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease-reduced risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased cutaneous melanoma risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased cutaneous melanoma risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease risk factors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease risk factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; fracture risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wegener's granulomatosis- reduced risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wegener's granulomatosis- reduced risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risk factors and tumor characteristics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease risk factors and tumor characteristics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cancer risk in hcv antibody-positive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cancer risk in hcv antibody-positive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular risk factors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular risk factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diet lifestyle and risk of colon cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diet lifestyle and risk of colon cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombotic risk factors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombotic risk factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risk-taking behavior in a gambling task Gene SetFrom GAD Gene-Disease Associations genes associated with the disease risk-taking behavior in a gambling task in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease risk factors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease risk factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sudden cardiac arrest risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sudden cardiac arrest risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased risk of cerebrovascular mortality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased risk of cerebrovascular mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial cancer risk. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risk of cervical dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease risk of cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
migraine risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease migraine risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
financial risk taking Gene SetFrom GAD Gene-Disease Associations genes associated with the disease financial risk taking in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increasing risk and a poor prognosis of renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increasing risk and a poor prognosis of renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer risk and prenatal viability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer risk and prenatal viability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced risk of restenosis after coronary stenting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced risk of restenosis after coronary stenting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risk Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term risk in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Suicide risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Suicide risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hypertension risk in short sleep duration Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Cardiovascular disease risk factors Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Cardiovascular disease risk factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
{macular degeneration, age-related, 14, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{colonic adenoma recurrence, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {colonic adenoma recurrence, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{macular degeneration, age-related, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malaria, cerebral, reduced risk of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{gastric cancer risk after h. pylori infection} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {gastric cancer risk after h. pylori infection} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Intermediate Risk Gastrointestinal Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intermediate Risk Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased Risk Of Sudden Cardiac Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Risk Of Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Risk Of Pancreatic Cancer Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Risk Of Pancreatic Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mortality risk in patients Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mortality risk in patients phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Risk of requirement of invasive mechanical ventilation in patients Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Risk of requirement of invasive mechanical ventilation in patients phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x quantitative lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x quantitative lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x quantitative lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x quantitative lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x dichotomous lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x dichotomous lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x dichotomous lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x dichotomous lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x quantitative lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x quantitative lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x quantitative lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x quantitative lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x dichotomous lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x dichotomous lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x dichotomous lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x dichotomous lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
End stage renal disease in APOL1 risk genotype-negative individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the End stage renal disease in APOL1 risk genotype-negative individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Self-reported risk-taking behaviour Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported risk-taking behaviour phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood protein levels in cardiovascular risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood protein levels in cardiovascular risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White matter integrity (bipolar disorder risk interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter integrity (bipolar disorder risk interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular disease risk factors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular disease risk factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Falling risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Falling risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Suicide risk Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicide risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular risk factors (age interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular risk factors (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular risk factors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular risk factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hypertension risk in short sleep duration Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 2 diabetes and end-stage kidney disease in APOL1 risk genotype negative individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes and end-stage kidney disease in APOL1 risk genotype negative individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Metabolite risk score for predicting weight gain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Metabolite risk score for predicting weight gain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
General risk tolerance (MTAG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the General risk tolerance (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Risk-taking tendency (4-domain principal component model) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Risk-taking tendency (4-domain principal component model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Symptoms in placebo-treated COVID-19 outpatients at risk of severe disease (time to remission) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Symptoms in placebo-treated COVID-19 outpatients at risk of severe disease (time to remission) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
high pressure neurological syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease high pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
High myopia-sensorineural deafness syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease High myopia-sensorineural deafness syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
High pressure neurological syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High myopia-sensorineural deafness syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High myopia-sensorineural deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High myopia-sensorineural deafness syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High myopia-sensorineural deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Deafness, high-frequency sensorineural, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, high-frequency sensorineural, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
High bone mass Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
spherical high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the spherical high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
discoidal high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the discoidal high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
high-affinity iron permease complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the high-affinity iron permease complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
spherical high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spherical high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
discoidal high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the discoidal high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
DJ-1-SNCA complex, high molecular weight complex Gene Setproteins in the DJ-1-SNCA complex, high molecular weight complex protein complex from the CORUM Protein Complexes dataset. |
ultra-high molecular weight polyethylene Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical ultra-high molecular weight polyethylene from the curated CTD Gene-Chemical Interactions dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 from the curated CTD Gene-Disease Associations dataset. |
Cardiac Output, High Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Output, High from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 from the curated CTD Gene-Disease Associations dataset. |
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset. |
high serum ige concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high serum ige concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glioma (high-grade) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glioma (high-grade) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high insulin concentrations in non-diabetic mexican ameri Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high insulin concentrations in non-diabetic mexican ameri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high ethanol tolerance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high ethanol tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma high density lipoprotein cholesterol and apolipoprotein ai Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma high density lipoprotein cholesterol and apolipoprotein ai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high density lipoprotein. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high density lipoprotein. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high plasma cetp activity. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high plasma cetp activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, high-frequency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; candidiasis; high-altitude illness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; candidiasis; high-altitude illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high density lipoprotein levels. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high density lipoprotein levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high triglyceride/ low hdl cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high triglyceride/ low hdl cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing disorders; hearing loss, high-frequency; hearing problem Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high plasma factor viii: c levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high plasma factor viii: c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high interleukin-1 beta plasma levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high interleukin-1 beta plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-density lipoprotein cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-density lipoprotein cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased circulating high density lipoprotein cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased circulating high density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high neuroticism and low agreeableness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high neuroticism and low agreeableness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low high-density lipoprotein cholesterol concentration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low high-density lipoprotein cholesterol concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high altitude performance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high altitude performance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymph node involvement and other histopathological indicators of high metastatic potential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymph node involvement and other histopathological indicators of high metastatic potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-density lipoprotein cholesterol level. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-density lipoprotein cholesterol level. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high frequency of factor v leiden mutation. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high frequency of factor v leiden mutation. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high density lipoprotein cholesterol level Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high density lipoprotein cholesterol level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma high-density lipoprotein cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma high-density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-grade soft tissue sarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-grade soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high exposure to aflatoxin b1. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high exposure to aflatoxin b1. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-altitude illness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-altitude illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-monounsaturated fatty acid diet Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-monounsaturated fatty acid diet in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high or low factor xiii specific activity. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high or low factor xiii specific activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high and low levels of cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high and low levels of cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-altitude pulmonary edema. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-altitude pulmonary edema. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high-density lipoprotein-cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high-density lipoprotein-cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high total ige Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high total ige in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high inducibility of cytochrome p450 1a1 gene transcription Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high inducibility of cytochrome p450 1a1 gene transcription in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2015 dataset. |
high-density lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the high-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to high density lipoprotein particle stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to high density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
lymphocyte chemotaxis across high endothelial venule Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lymphocyte chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to high density lipoprotein particle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to high density lipoprotein particle biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
b cell chemotaxis across high endothelial venule Gene SetFrom GO Biological Process Annotations 2015 genes participating in the b cell chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations 2015 dataset. |
high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
spherical high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the spherical high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
discoidal high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the discoidal high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
high-affinity l-ornithine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity l-ornithine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity lysine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-density lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-density lipoprotein particle receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-density lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity basic amino acid transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high molecular weight b cell growth factor receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high molecular weight b cell growth factor receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity inorganic phosphate:sodium symporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity inorganic phosphate:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-density lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity arginine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity glutamate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
high-affinity oligopeptide transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the high-affinity oligopeptide transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Blood pressure measurement (high sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure measurement (high sodium and potassium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Glioma (high-grade) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Glioma (high-grade) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
high-frequency hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the high-frequency hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high iliac wings Gene SetFrom HPO Gene-Disease Associations genes associated with the high iliac wings phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high palate Gene SetFrom HPO Gene-Disease Associations genes associated with the high palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high axial triradius Gene SetFrom HPO Gene-Disease Associations genes associated with the high axial triradius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high nonceruloplasmin-bound serum copper Gene SetFrom HPO Gene-Disease Associations genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high maternal serum alpha-fetoprotein Gene SetFrom HPO Gene-Disease Associations genes associated with the high maternal serum alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high, narrow palate Gene SetFrom HPO Gene-Disease Associations genes associated with the high, narrow palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high-frequency sensorineural hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the high-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high-output congestive heart failure Gene SetFrom HPO Gene-Disease Associations genes associated with the high-output congestive heart failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high anterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the high anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high pitched voice Gene SetFrom HPO Gene-Disease Associations genes associated with the high pitched voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high forehead Gene SetFrom HPO Gene-Disease Associations genes associated with the high forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high-grade hypermetropia Gene SetFrom HPO Gene-Disease Associations genes associated with the high-grade hypermetropia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hearing Loss, High-Frequency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
High affinity immunoglobulin epsilon receptor subunit beta Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High affinity immunoglobulin epsilon receptor subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
T-cell surface glycoprotein CD3 zeta/eta subunit/High affinity IgE receptor gamma subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the T-cell surface glycoprotein CD3 zeta/eta subunit/High affinity IgE receptor gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Keratin, high-sulphur matrix protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Keratin, high-sulphur matrix protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group box domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group, HMG-I/HMG-Y Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group nucleosome-binding domain-containing family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group box domain 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
high palate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the high palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
high mean erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the high mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ly6c high monocyte number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased ly6c high monocyte number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[high density lipoprotein cholesterol level qtl 4] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset. |
{high density lipoprotein cholesterol, low serum, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {high density lipoprotein cholesterol, low serum, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 2] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset. |
[hemoglobin, high altitude adaptation] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [hemoglobin, high altitude adaptation] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 8] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 8] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high molecular weight kininogen deficiency] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high molecular weight kininogen deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 12] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 12] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 10] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 10] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 5] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 1] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[gamma-glutamyltransferase, familial high serum] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 9] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 9] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl6] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl6] phenotype from the curated OMIM Gene-Disease Associations dataset. |
b-cell non-hodgkin lymphoma, high-grade Gene SetFrom OMIM Gene-Disease Associations genes associated with the b-cell non-hodgkin lymphoma, high-grade phenotype from the curated OMIM Gene-Disease Associations dataset. |
high density lipoprotein cholesterol level qtl14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the high density lipoprotein cholesterol level qtl14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[high density lipoprotein cholesterol level qtl 11] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [high density lipoprotein cholesterol level qtl 11] phenotype from the curated OMIM Gene-Disease Associations dataset. |
{high density lipoprotein cholesterol level qtl 7} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {high density lipoprotein cholesterol level qtl 7} phenotype from the curated OMIM Gene-Disease Associations dataset. |
high endothelial venule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue high endothelial venule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
high vocal center Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue high vocal center in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
High Density Lipoprotein Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Density Lipoprotein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Grade Prostatic Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade Prostatic Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade B-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade B-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Altitude Cerebral Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Altitude Pulmonary Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Pulmonary Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Altitude Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Lymphoma (Neoplasm) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Lymphoma (Neoplasm) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microsatellite Instability-High Colorectal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microsatellite Instability-High Colorectal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Output Heart Failure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Output Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Serous Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Serous Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Renin Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Renin Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Msi-High Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Msi-High in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical High Grade Squamous Intraepithelial Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical High Grade Squamous Intraepithelial Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Cervical Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Cervical Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Astrocytic Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Astrocytic Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade B-Cell Lymphoma, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade B-Cell Lymphoma, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade B-Cell Non-Hodgkin'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade B-Cell Non-Hodgkin'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Stromal Sarcoma, High Grade Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Stromal Sarcoma, High Grade in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uterine Corpus High Grade Endometrial Stromal Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uterine Corpus High Grade Endometrial Stromal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade T-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Grade Salivary Gland Mucoepidermoid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade Salivary Gland Mucoepidermoid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Output Congestive Heart Failure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Output Congestive Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Dysplastic Nodule Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Dysplastic Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Liver Dysplastic Nodule Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Liver Dysplastic Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Grade Salivary Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade Salivary Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Functioning Autism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Functioning Autism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Molecular Weight Kininogen Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Molecular Weight Kininogen Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Frequency Sensorineural Hearing Impairment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Frequency Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Axial Triradius Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Axial Triradius in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucoepidermoid Carcinoma, High Grade Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucoepidermoid Carcinoma, High Grade in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Oxygen-Affinity Hemoglobin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Oxygen-Affinity Hemoglobin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal High Grade Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal High Grade Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Grade Neuroendocrine Carcinoma Of Cervix Uteri Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade Neuroendocrine Carcinoma Of Cervix Uteri in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microsatellite Instability-High Solid Malignant Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microsatellite Instability-High Solid Malignant Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Astigmatism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Astigmatism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Turnover Bone Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Turnover Bone Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Surface Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Surface Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Renin Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Renin Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycythemia Due To High Altitude Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To High Altitude in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Forehead Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Forehead in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Pitched Cry Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Pitched Cry in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Density Lipoprotein Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Density Lipoprotein Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High, Narrow Palate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High, Narrow Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Lipids High (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Lipids High (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Pitched Voice Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Pitched Voice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High-Grade Squamous Intraepithelial Lesions Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High-Grade Squamous Intraepithelial Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Anterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Anterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Density Lipoprotein Cholesterol Level Quantitative Trait Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Density Lipoprotein Cholesterol Level Quantitative Trait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Iliac Wings Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Iliac Wings in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Nonceruloplasmin-Bound Serum Copper Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Nonceruloplasmin-Bound Serum Copper in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Bone Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Bone Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Myoinositol In Brain By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Myoinositol In Brain By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cardiac Output, High Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Output, High in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
negative regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2023 dataset. |
lymphocyte chemotaxis across high endothelial venule Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lymphocyte chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
high-density lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the high-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2023 dataset. |
high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2023 genes participating in the calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to high density lipoprotein particle stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to high density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
discoidal high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the discoidal high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
spherical high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the spherical high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
high voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity L-glutamate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity L-glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-density lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-density lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity IgG receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity IgG receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity IgE receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity IgE receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity L-arginine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity L-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity lysine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high-affinity basic amino acid transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the high-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
high mean erythrocyte cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the high mean erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
high forehead Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the high forehead phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
high palate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the high palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased CD11b-high dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased CD11b-high dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased Ly6C high monocyte number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased Ly6C high monocyte number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased CD11b-high dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased CD11b-high dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased Ly6C high monocyte number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased Ly6C high monocyte number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
high preference for an addictive substance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the high preference for an addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased Ly6C high monocyte number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased Ly6C high monocyte number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased CD11b-high dendritic cell number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased CD11b-high dendritic cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased CD11b-high dendritic cell number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased CD11b-high dendritic cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased Ly6C high monocyte number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased Ly6C high monocyte number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
High-endothelial venule (HEV) cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the High-endothelial venule (HEV) cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells Gene Setproteins participating in the High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells pathway from the Reactome Pathways 2024 dataset. |
Signaling by high-kinase activity BRAF mutants Gene Setproteins participating in the Signaling by high-kinase activity BRAF mutants pathway from the Reactome Pathways 2024 dataset. |
Large intestine_CT1_ILV high endothelial venule endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_ILV high endothelial venule endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_ILV high endothelial venule endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_ILV high endothelial venule endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
negative regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2025 dataset. |
lymphocyte chemotaxis across high endothelial venule Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lymphocyte chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
high-density lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the high-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2025 dataset. |
high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of high-density lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of high voltage-gated calcium channel activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2025 genes participating in the calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to high density lipoprotein particle stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to high density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of calcium ion transmembrane transport via high voltage-gated calcium channel Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of calcium ion transmembrane transport via high voltage-gated calcium channel biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to high light intensity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to high light intensity biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of high-density lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
discoidal high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the discoidal high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
spherical high-density lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the spherical high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
high voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity L-glutamate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity L-glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity IgM receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity IgM receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-density lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-density lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity IgG receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity IgG receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity IgE receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity IgE receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity L-arginine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity L-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity lysine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
high-affinity basic amino acid transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the high-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
High grade glioma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease High grade glioma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
High grade glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
T2-high asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T2-high asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High grade ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High grade ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High molecular weight kininogen deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High molecular weight kininogen deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
high-grade astrocytoma with piloid features Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease high-grade astrocytoma with piloid features in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
high-grade B-cell lymphoma double-hit/triple-hit Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease high-grade B-cell lymphoma double-hit/triple-hit in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High endothelial venule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue High endothelial venule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
High vocal center Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue High vocal center in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
para-high vocal center Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue para-high vocal center in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Spherical high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Spherical high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Discoidal high-density lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Discoidal high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Discoidal high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Discoidal high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spherical high-density lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spherical high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
high-affinity iron permease complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the high-affinity iron permease complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
High grade surface osteosarcoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High grade surface osteosarcoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High bone mass Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High density lipoprotein cholesterol level quantitative trait locus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High density lipoprotein cholesterol level quantitative trait locus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High palate Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High palate phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High molecular weight kininogen deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High molecular weight kininogen deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pediatric high-grade glioma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pediatric high-grade glioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial High Density Lipoprotein Deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial High Density Lipoprotein Deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High-grade astrocytoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High-grade astrocytoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High myopia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the High myopia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
High light scatter reticulocyte count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High light scatter reticulocyte count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High light scatter reticulocyte percentage of red cells Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High light scatter reticulocyte percentage of red cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum C-reactive protein concentration in high fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C-reactive protein concentration in high fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High myopia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High myopia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Postprandial triglyceride response to high fat diet meal Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Postprandial triglyceride response to high fat diet meal phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High fetal hemoglobin in sickle cell disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High fetal hemoglobin in sickle cell disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glaucoma (high intraocular pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glaucoma (high intraocular pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low high density lipoprotein cholesterol levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low high density lipoprotein cholesterol levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Age-related hearing impairment (high frequency) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related hearing impairment (high frequency) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High fasting blood glucose Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High fasting blood glucose phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High density lipoprotein cholesterol levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High density lipoprotein cholesterol levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in heavy smokers (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in heavy smokers (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in never smokers (high FEV1 vs average FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in never smokers (high FEV1 vs average FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in heavy smokers (high FEV1 vs average FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in heavy smokers (high FEV1 vs average FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in never smokers (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in never smokers (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
B-cell acute lymphoblastic leukaemia (high-hyperdiploidy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the B-cell acute lymphoblastic leukaemia (high-hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gemcitabine-induced early high-grade neutropenia in pancreatic cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gemcitabine-induced early high-grade neutropenia in pancreatic cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glioma (high-grade) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glioma (high-grade) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High serum lipase activity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High serum lipase activity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (high sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (high sodium and potassium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Psychological resilience (outcome-based) in high deployment stress exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Psychological resilience (outcome-based) in high deployment stress exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High-sensitivity C-reactive protein levels in HIV infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High-sensitivity C-reactive protein levels in HIV infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High-sensitivity cardiac troponin T levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High-sensitivity cardiac troponin T levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Extremely high intelligence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Extremely high intelligence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subclinical trait of interstitial lung disease (basilar percentage of high attenuation areas on CT scan) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subclinical trait of interstitial lung disease (basilar percentage of high attenuation areas on CT scan) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subclinical trait of interstitial lung disease (percentage of high attenuation areas on CT scan) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subclinical trait of interstitial lung disease (percentage of high attenuation areas on CT scan) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High altitude adaptation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High altitude adaptation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High chromosomal aberration frequency (chromatid type) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromatid type) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High chromosomal aberration frequency (chromosome type) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromosome type) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High chromosomal aberration frequency (total) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (total) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High chromosomal aberration frequency (chromatid type) in genotoxic compound exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromatid type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
High-grade serous ovarian cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High-grade serous ovarian cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC2866657-pone.0010547.s001.xls-ERG-high-GENES_DOWNREGULATED_IN_ERGhigh_ERG Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC2866657-pone.0010547.s001.xls-ERG-high-GENES_DOWNREGULATED_IN_ERGhigh_ERG transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
PMC2866657-pone.0010547.s001.xls-ERG-high-GENES_UPREGULATED_IN_ERGhigh_ERG Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC2866657-pone.0010547.s001.xls-ERG-high-GENES_UPREGULATED_IN_ERGhigh_ERG transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
PMC11749115-loae020_suppl_Supplementary_Table_S2.xlsx-CHOP-high-gene_DDIT3 Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC11749115-loae020_suppl_Supplementary_Table_S2.xlsx-CHOP-high-gene_DDIT3 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Lynch syndrome:Turcot syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marfan's syndrome:Marfan's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
IFAP syndrome with or without BRESHECK syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome I:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset. |
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset. |
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome 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 SetFrom 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. |
cornelia de lange syndrome; de lange syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatigue syndrome, chronic; fatigue syndrome; postviral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom 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. |
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
restless legs syndrome; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; uveomeningoencephalitic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melas syndrome; merrf syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene SetFrom 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. |
angelman syndrome; rett syndrome; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult 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 SetFrom 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. |
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
metabolic syndrome ; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
digeorge syndrome; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome 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 SetFrom 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. |
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene SetFrom 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. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
down syndrome; ehlers-danlos syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart-hand syndrome, holt-oram syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
digeorge syndrome/velocardiofacial syndrome complex-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ifap syndrome with or without bresheck syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Crouzon syndrome-acanthosis nigricans syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crouzon syndrome-acanthosis nigricans syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Crouzon syndrome-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
Branchiootic syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branchiootic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome, type 3, with hypocalciuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple synostoses syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sjögren-Larsson syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sjögren-Larsson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hennekam lymphangiectasia-lymphedema syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hennekam lymphangiectasia-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
UV-sensitive syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the UV-sensitive syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib-polydactyly syndrome, Majewski type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Char syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Char syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fragile X syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fragile X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Shwachman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Shwachman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Greig cephalopolysyndactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Greig cephalopolysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Melnick-Fraser syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Melnick-Fraser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marfan's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Melnick-Needles syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Melnick-Needles syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Branchiootorenal syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branchiootorenal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PTEN hamartoma tumor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PTEN hamartoma tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lesch-Nyhan syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lesch-Nyhan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oculofaciocardiodental syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oculofaciocardiodental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Robinow Sorauf syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Robinow Sorauf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
17q2131 microdeletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 17q2131 microdeletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Desbuquois syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Desbuquois syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly/autism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly/autism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, type 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, type 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mohr-Tranebjaerg syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mohr-Tranebjaerg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Osteopenic nonfracture syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Osteopenic nonfracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Barakat syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Barakat syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Raine syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Raine syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digitorenocerebral syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Digitorenocerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ataxia-telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alport syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alstrom syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alstrom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinism-hyperammonemia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal multiple pterygium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MORM syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MORM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Upshaw-Schulman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Upshaw-Schulman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Martsolf syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Martsolf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chromosome 2q32-q33 deletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blepharophimosis-ptosis-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Borrone Di Rocco Crovato syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Borrone Di Rocco Crovato syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hurler syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hurler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angelman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angelman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lig4 syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lig4 syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rubinstein-Taybi syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hajdu-Cheney syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hajdu-Cheney syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperferritinemia cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Temtamy preaxial brachydactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Temtamy preaxial brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin E syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bannayan-Riley-Ruvalcaba syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bannayan-Riley-Ruvalcaba syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chudley-McCullough syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chudley-McCullough syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poretti-boltshauser syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poretti-boltshauser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frank Ter Haar syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frank Ter Haar syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Androgen resistance syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoparathyroidism retardation dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holt-Oram syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holt-Oram syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Duane syndrome type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Young Simpson syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Young Simpson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frasier syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frasier syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
C-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meier-Gorlin syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meier-Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pili torti-deafness syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pili torti-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gorlin syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marshall syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marshall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carpenter syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bernard-Soulier syndrome, type A2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Duane-radial ray syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Duane-radial ray syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bardet-Biedl syndrome 19 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
22q133 deletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 22q133 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa-corneal clouding-oligophrenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bardet-Biedl syndrome 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TNF receptor-associated periodic fever syndrome (TRAPS) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Waardenburg syndrome type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Steel syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Steel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chromosome 1q43-q44 deletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Roberts-SC phocomelia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Roberts-SC phocomelia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bloom syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bloom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
McLeod neuroacanthocytosis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the McLeod neuroacanthocytosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebrooculofacioskeletal syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebrooculofacioskeletal syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nicolaides-Baraitser syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nicolaides-Baraitser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nager syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nager syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chédiak-Higashi syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chédiak-Higashi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kindler's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kindler's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnevale syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnevale syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kenny syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kenny syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic pain syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rienhoff syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rienhoff syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Weaver syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Weaver syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia/short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Siderius X-linked mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kohlschutter's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kohlschutter's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with marfanoid habitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebro-oculo-facio-skeletal syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebro-oculo-facio-skeletal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis-lymphedema-telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LEOPARD syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LEOPARD syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Treacher collins syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Treacher collins syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wiskott-Aldrich syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wiskott-Aldrich syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic pain syndrome, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyper-IgE syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyper-IgE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tourette Syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tourette Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, macrosomia, facial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome antenatal type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome antenatal type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamstorp-Wohlfart syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamstorp-Wohlfart syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Turcot syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sick sinus syndrome 2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyaline fibromatosis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyaline fibromatosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity and multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, and endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Weill-Marchesani-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Weill-Marchesani-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Netherton syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Netherton syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome, type 4b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Feingold syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Feingold syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Waardenburg syndrome type 4B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Richieri Costa Pereira syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Richieri Costa Pereira syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoimmune lymphoproliferative syndrome, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, fast-channel Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wilson-Turner X-linked mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Costello syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Costello syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ochoa syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ochoa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bruck syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bruck syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Achalasia-alacrima syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Achalasia-alacrima syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cryptophthalmos syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cryptophthalmos syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nijmegen breakage syndrome-like disorder Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brugada syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brugada syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brugada syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brugada syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brugada syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ovarian hyperstimulation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ovarian hyperstimulation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Otofaciocervical syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Otofaciocervical syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kaufman oculocerebrofacial syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kaufman oculocerebrofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stickler syndrome, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stickler syndrome, type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stickler syndrome, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Branchiooculofacial syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branchiooculofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Karak syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Karak syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky Pudlak syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky Pudlak syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tarsal carpal coalition syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tarsal carpal coalition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jankovic Rivera syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jankovic Rivera syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nakajo syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nakajo syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chromosome Xq28 deletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi-Bickel syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi-Bickel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
short QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Smith-Lemli-Opitz syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Smith-Lemli-Opitz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Von Hippel-Lindau syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1G Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome progeroid type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Larsen syndrome, dominant type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome, musculocontractural type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Temtamy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Temtamy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Birk Barel mental retardation dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alport syndrome, X-linked recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasia with mental retardation syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasia with mental retardation syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasia with mental retardation syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasia with mental retardation syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasia with mental retardation syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenomatous polyposis coli:Gardner syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenomatous polyposis coli:Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal congenital contracture syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leprechaunism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leprechaunism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Simpson-Golabi-Behmel syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Simpson-Golabi-Behmel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
XFE progeroid syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the XFE progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dysequilibrium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dysequilibrium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atypical hemolytic-uremic syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atypical hemolytic-uremic syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Johanson-Blizzard syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Johanson-Blizzard syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GRACILE syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GRACILE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked lymphoproliferative syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kowarski syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kowarski syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ADULT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the ADULT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel-Gruber syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel-Gruber syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked lymphoproliferative syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neutrophil immunodeficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutrophil immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coffin-Lowry syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coffin-Lowry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Auriculocondylar syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Auriculocondylar syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Auriculocondylar syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome, hydroxylysine-deficient Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, hydroxylysine-deficient phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pierson syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pierson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pfeiffer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pfeiffer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Loeys-Dietz syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tricho-dento-osseous syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tricho-dento-osseous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mowat-Wilson syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mowat-Wilson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, type 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Perrault syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Perrault syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jensen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jensen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Werner syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Werner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aarskog syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aarskog syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Enamel-renal syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Enamel-renal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 21 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 22 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple synostoses syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Popliteal pterygium syndrome lethal type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Keutel syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Keutel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pitt-Hopkins syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Segawa syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Segawa syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple pterygium syndrome Escobar type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pitt-Hopkins-like syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pitt-Hopkins-like syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital short bowel syndrome, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
C syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the C syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Klippel-Feil syndrome 2, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stiff skin syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stiff skin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lenz microphthalmia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lenz microphthalmia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marshall/Stickler syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marshall/Stickler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schwartz Jampel syndrome type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Grebe syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Grebe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Saethre-Chotzen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Saethre-Chotzen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, slow-channel congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Floating-Harbor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Floating-Harbor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warburg micro syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warburg micro syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warburg micro syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hermansky-Pudlak syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Osler hemorrhagic telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Osler hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wieacker syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wieacker syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kabuki make-up syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kabuki make-up syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cohen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cohen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oligodontia-colorectal cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oligodontia-colorectal cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Filippi syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Filippi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal congenital contractural syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primrose syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primrose syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Perrault syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marshall-Smith syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marshall-Smith syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Loeys-Dietz syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brittle cornea syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brittle cornea syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rotor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rotor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oral-facial-digital syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oral-facial-digital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acrocallosal syndrome, Schinzel type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gray platelet syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gray platelet syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mast syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mast syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Amish infantile epilepsy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meacham syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meacham syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stormorken syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stormorken syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Opitz-Frias syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Opitz-Frias syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardio-facio-cutaneous syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardio-facio-cutaneous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kallmann syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kallmann syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kallmann syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kallmann syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kallmann syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Yunis Varon syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Yunis Varon syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mulibrey nanism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mulibrey nanism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ohdo syndrome, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ohdo syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, idiopathic, steroid-resistant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Townes-Brocks-branchiootorenal-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Townes-Brocks-branchiootorenal-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SeSAME syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SeSAME syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Odontotrichomelic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Odontotrichomelic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Meckel syndrome, type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile liver failure syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile liver failure syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lowe syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lowe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome, type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos syndrome, musculocontractural type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rett syndrome, congenital variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Van Maldergem syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Robinow syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Orofaciodigital syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Orofaciodigital syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distichiasis-lymphedema syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distichiasis-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Townes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Townes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neu-Laxova syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neu-Laxova syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Winchester syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Winchester syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Unverricht-Lundborg syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Unverricht-Lundborg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Verheij syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Verheij syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rapp-Hodgkin ectodermal dysplasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Allan-Herndon-Dudley syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Allan-Herndon-Dudley syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced sleep phase syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sick sinus syndrome 1, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arterial tortuosity syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arterial tortuosity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Papillon-Lefèvre syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Papillon-Lefèvre syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brown-vialetto-van laere syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brown-vialetto-van laere syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peters plus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peters plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulnar-mammary syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulnar-mammary syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-dependent diabetes mellitus secretory diarrhea syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-dependent diabetes mellitus secretory diarrhea syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Zunich neuroectodermal syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Beckwith-Wiedemann syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Beckwith-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Van Maldergem Wetzburger Verloes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem Wetzburger Verloes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sotos' syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sotos' syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dyggve-Melchior-Clausen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dyggve-Melchior-Clausen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Baraitser-Winter Syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Baraitser-Winter Syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Three M syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Three M syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Howel-Evans syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Howel-Evans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Senior-Loken syndrome 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Senior-Loken syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Senior-Loken syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rhabdoid tumor predisposition syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Finnish congenital nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tatton-Brown-rahman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tatton-Brown-rahman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
COACH syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the COACH syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib polydactyly syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib polydactyly syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Enhanced s-cone syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Enhanced s-cone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Van der Woude syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Van der Woude syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |