Name

two carpal ossification centers present at birth Gene Set

From HPO Gene-Disease Associations

genes associated with the two carpal ossification centers present at birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Two Carpal Ossification Centers Present At Birth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Two Carpal Ossification Centers Present At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

multiple carpal ossification centers Gene Set

From HPO Gene-Disease Associations

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

Multiple Carpal Ossification Centers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Carpal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

femoral bowing present at birth, straightening with time Gene Set

From HPO Gene-Disease Associations

genes associated with the femoral bowing present at birth, straightening with time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Femoral Bowing Present At Birth, Straightening With Time Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Femoral Bowing Present At Birth, Straightening With Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

fused sternal ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the fused sternal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large sternal ossification centers Gene Set

From HPO Gene-Disease Associations

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

supernumerary vertebral ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the supernumerary vertebral ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Supernumerary Vertebral Ossification Centers Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Supernumerary Vertebral Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fused Sternal Ossification Centers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fused Sternal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Large Sternal Ossification Centers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Large Sternal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

severe carpal ossification delay Gene Set

From HPO Gene-Disease Associations

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

advanced ossification of carpal bones Gene Set

From HPO Gene-Disease Associations

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

abnormality of carpal bone ossification Gene Set

From HPO Gene-Disease Associations

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

delayed ossification of carpal bones Gene Set

From HPO Gene-Disease Associations

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

Advanced Ossification Of Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Advanced Ossification Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Ossification Of Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Ossification Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Severe Carpal Ossification Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Severe Carpal Ossification Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

birth weight; infant, newborn, diseases; infection; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; premature birth Gene Set

From GAD Gene-Disease Associations

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

Spontaneous preterm birth (preterm birth) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Spontaneous preterm birth (preterm birth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

ossification of posterior longitudinal ligament; ossification, heterotopic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ossification of posterior longitudinal ligament; ossification, heterotopic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

present Gene Set

From GeneRIF Biological Term Annotations

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

Increased Cellularity Present Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Increased Cellularity Present in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Nasal Obstruction Present Finding Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Nasal Obstruction Present Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

centers Gene Set

From GeneRIF Biological Term Annotations

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

proton-transporting two-sector atpase complex, proton-transporting domain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting two-sector atpase complex, proton-transporting domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting two-sector atpase complex, catalytic domain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting two-sector atpase complex, catalytic domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting two-sector atpase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting two-sector atpase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting two-sector atpase complex, catalytic domain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting two-sector atpase complex, catalytic domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proton-transporting two-sector atpase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting two-sector atpase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proton-transporting two-sector atpase complex, proton-transporting domain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting two-sector atpase complex, proton-transporting domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

two major non-ribosomal nucleolar proteins and its implication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease two major non-ribosomal nucleolar proteins and its implication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

two-hour glucose challenge Gene Set

From GAD Gene-Disease Associations

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

proton-transporting two-sector atpase complex assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the proton-transporting two-sector atpase complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

proton-transporting two-sector atpase complex, proton-transporting domain Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the proton-transporting two-sector atpase complex, proton-transporting domain cellular component from the curated GO Cellular Component Annotations 2015 dataset.

proton-transporting two-sector atpase complex, catalytic domain Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the proton-transporting two-sector atpase complex, catalytic domain cellular component from the curated GO Cellular Component Annotations 2015 dataset.

proton-transporting two-sector atpase complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the proton-transporting two-sector atpase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2015 dataset.

Two-hour glucose challenge Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Two-hour glucose challenge phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Two pore domain potassium channel, TWIK-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TWIK-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, THIK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, THIK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TRAAK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TRAAK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TASK family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TASK family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pantothenate kinase, acetyl-CoA regulated, two-domain type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pantothenate kinase, acetyl-CoA regulated, two-domain type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TREK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TREK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TWIK family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore calcium channel protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore calcium channel protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore calcium channel protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore calcium channel protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Klinefelter'S Syndrome - Male With More Than Two X Chromosomes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Klinefelter'S Syndrome - Male With More Than Two X Chromosomes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Two-Raphe Bicuspid Aortic Valve Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Two-Raphe Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

proton-transporting two-sector ATPase complex assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the proton-transporting two-sector ATPase complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2023 dataset.

proton-transporting two-sector ATPase complex assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the proton-transporting two-sector ATPase complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2025 dataset.

proton-transporting two-sector ATPase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the proton-transporting two-sector ATPase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

proton-transporting two-sector ATPase complex, catalytic domain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the proton-transporting two-sector ATPase complex, catalytic domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

proton-transporting two-sector ATPase complex, proton-transporting domain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the proton-transporting two-sector ATPase complex, proton-transporting domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

proton-transporting two-sector ATPase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the proton-transporting two-sector ATPase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

proton-transporting two-sector ATPase complex, catalytic domain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the proton-transporting two-sector ATPase complex, catalytic domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

proton-transporting two-sector ATPase complex, proton-transporting domain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the proton-transporting two-sector ATPase complex, proton-transporting domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Two-hour glucose Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Two-hour glucose phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Two-hour glucose in pregnancy (gestational week 30-32) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Two-hour glucose in pregnancy (gestational week 30-32) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Two-hour glucose challenge Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Two-hour glucose challenge phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Tarsal carpal coalition syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tarsal carpal coalition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carpal Tunnel Syndrome Gene Set

From CTD Gene-Disease Associations

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

carpal tunnel syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

carpal tunnel syndrome; Gene Set

From GAD Gene-Disease Associations

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

carpal-tunnel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carpal-tunnel syndrome 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 Set

From 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.

carpal Gene Set

From GeneRIF Biological Term Annotations

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

accessory carpal bones Gene Set

From HPO Gene-Disease Associations

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

malaligned carpal bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of the carpal bones Gene Set

From HPO Gene-Disease Associations

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

abnormal calcification of the carpal bones Gene Set

From HPO Gene-Disease Associations

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

irregular carpal bones Gene Set

From HPO Gene-Disease Associations

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

carpal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

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

carpal osteolysis Gene Set

From HPO Gene-Disease Associations

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

crowded carpal bones Gene Set

From HPO Gene-Disease Associations

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

carpal bone aplasia Gene Set

From HPO Gene-Disease Associations

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

carpal synostosis Gene Set

From HPO Gene-Disease Associations

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

stippled calcification in carpal bones Gene Set

From HPO Gene-Disease Associations

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

abnormally shaped carpal bones Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the carpal bones Gene Set

From HPO Gene-Disease Associations

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

synostosis of carpal bones Gene Set

From HPO Gene-Disease Associations

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

Carpal Tunnel Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

fused carpal bones Gene Set

From MPO Gene-Phenotype Associations

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

absent carpal bone Gene Set

From MPO Gene-Phenotype Associations

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

abnormal carpal bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

carpal tunnel syndrome, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

tarsal-carpal coalition syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the tarsal-carpal coalition syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Tarsal-Carpal Coalition Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Tarsal-Carpal Coalition Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Carpal Tunnel Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Carpal Tunnel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Carpal Synostosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Carpal Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Irregular Carpal Bones Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Irregular Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Accessory Carpal Bones Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Accessory Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Synostosis, Carpal, With Dysplastic Elbow Joints And Brachydactyly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Synostosis, Carpal, With Dysplastic Elbow Joints And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bilateral Carpal Tunnel Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bilateral Carpal Tunnel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Carpal Tunnel Syndrome, Familial Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Carpal Tunnel Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Carpal Bone Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Carpal Bone Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Synostosis Of Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Synostosis Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of The Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Calcification Of The Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Calcification Of The Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Stippled Calcification In Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Stippled Calcification In Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormally Shaped Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormally Shaped Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Malaligned Carpal Bone Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Malaligned Carpal Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Carpal Bone Aplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Carpal Bone Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Carpal Osteolysis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Carpal Osteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Crowded Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Crowded Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Aplasia/Hypoplasia Involving The Carpal Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Aplasia/Hypoplasia Involving The Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormal carpal bone morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal carpal bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

fused carpal bones Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the fused carpal bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent carpal bone Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent carpal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Carpal tunnel syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Carpal tunnel syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

tarsal-carpal coalition syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease tarsal-carpal coalition syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Carpal tunnel syndrome Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Carpal tunnel syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Carpal tunnel syndrome 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Carpal tunnel syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Carpal tunnel syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Carpal tunnel syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

tarsal-carpal coalition syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease tarsal-carpal coalition syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Carpal tunnel syndrome 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Carpal tunnel syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Tarsal-carpal coalition syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Tarsal-carpal coalition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Carpal tunnel syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Carpal tunnel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Carpal tunnel syndrome Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Carpal tunnel syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Premature Birth Gene Set

From CTD Gene-Disease Associations

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

Birth Weight Gene Set

From CTD Gene-Disease Associations

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

Birth Weight Gene Set

From dbGAP Gene-Trait Associations

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

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; growth disorders Gene Set

From GAD Gene-Disease Associations

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

birth weight; disorders Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hyperbilirubinemia, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

birth weight; growth disorders; insulin resistance Gene Set

From GAD Gene-Disease Associations

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

birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

premature birth; uterine cervical incompetence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth; uterine cervical incompetence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; premature birth; uterine prolapse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; premature birth; uterine prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

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

muscle testing; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight preterm delivery Gene Set

From GAD Gene-Disease Associations

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

spontaneous preterm birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chorioamnionitis; infection; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chorioamnionitis; infection; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus, type 1 Gene Set

From GAD Gene-Disease Associations

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

birth weight; insulin resistance Gene Set

From GAD Gene-Disease Associations

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

fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; weight gain Gene Set

From GAD Gene-Disease Associations

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

birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth defects Gene Set

From GAD Gene-Disease Associations

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

birth weight; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

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

birth weight; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

size at birth Gene Set

From GAD Gene-Disease Associations

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

chorioamnionitis; premature birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; hyperglycemia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

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

infection; inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

premature birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus, type 1; Gene Set

From GAD Gene-Disease Associations

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

birth weight; retinopathy of prematurity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; placenta diseases; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; placenta diseases; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial vaginosis; premature birth; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial vaginosis; premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; premature birth Gene Set

From GAD Gene-Disease Associations

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

birth weight; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

birth height growth to adolescence and adult stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth height growth to adolescence and adult stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cord blood igf-ii levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cord blood igf-ii levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight Gene Set

From GAD Gene-Disease Associations

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

body mass; birth weight; height Gene Set

From GAD Gene-Disease Associations

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

birth weight and serum triglyceride concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight and serum triglyceride concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; preterm delivery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; preterm delivery 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 Set

From 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.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dental plaque; periodontitis; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; periodontitis; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; critical illness Gene Set

From GAD Gene-Disease Associations

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

birth weight; body weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; cardiovascular disease; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; placental weight Gene Set

From GAD Gene-Disease Associations

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

chorioamnionitis; infection of amniotic sac and membranes; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

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

birth weight; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; patent ductus arteriosus; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; patent ductus arteriosus; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

preterm birth Gene Set

From GAD Gene-Disease Associations

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

body mass; diabetes, type 2; glucose; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cystic fibrosis; ileus Gene Set

From GAD Gene-Disease Associations

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

birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hellp syndrome; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hypertension Gene Set

From GAD Gene-Disease Associations

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

birth Gene Set

From GeneRIF Biological Term Annotations

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

embryo development ending in birth or egg hatching Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2015 dataset.

Birth weight Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of prenatal development or birth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

birth length less than 3rd percentile Gene Set

From HPO Gene-Disease Associations

genes associated with the birth length less than 3rd percentile phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prenatal development or birth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature birth following premature rupture of fetal membranes Gene Set

From HPO Gene-Disease Associations

genes associated with the premature birth following premature rupture of fetal membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

birth length greater than 97th percentile Gene Set

From HPO Gene-Disease Associations

genes associated with the birth length greater than 97th percentile phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature birth Gene Set

From HPO Gene-Disease Associations

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

desquamation of skin soon after birth Gene Set

From HPO Gene-Disease Associations

genes associated with the desquamation of skin soon after birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized muscular appearance from birth Gene Set

From HPO Gene-Disease Associations

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

Premature Birth Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Birth Weight Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

increased birth body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eyelids open at birth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the eyelids open at birth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal birth body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased birth weight Gene Set

From MPO Gene-Phenotype Associations

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

decreased birth body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal birth weight Gene Set

From MPO Gene-Phenotype Associations

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

decreased birth weight Gene Set

From MPO Gene-Phenotype Associations

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

[birth weight qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl4] phenotype from the curated OMIM Gene-Disease Associations dataset.

Infant, Very Low Birth Weight Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Infant, Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Alcohol Related Birth Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormality Of Prenatal Development Or Birth Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of Prenatal Development Or Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Patent Ductus Arteriosus After Birth At Term Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Patent Ductus Arteriosus After Birth At Term in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Premature Birth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Premature Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Birth Weight Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Very Low Birth Weight Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Desquamation Of Skin Soon After Birth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Desquamation Of Skin Soon After Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Birth Length Less Than 3Rd Percentile Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Birth Length Less Than 3Rd Percentile in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Generalized Muscular Appearance From Birth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Generalized Muscular Appearance From Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Infant, Extremely Low Birth Weight Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Infant, Extremely Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cephalhematoma Due To Birth Trauma Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cephalhematoma Due To Birth Trauma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Premature Birth Following Premature Rupture Of Fetal Membranes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Premature Birth Following Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Birth Length Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Birth Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Birth Length Greater Than 97Th Percentile Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Birth Length Greater Than 97Th Percentile in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Red, Cracking, Peeling Skin At Birth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Red, Cracking, Peeling Skin At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

embryo development ending in birth or egg hatching Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2023 dataset.

decreased birth body size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

eyelids open at birth Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the eyelids open at birth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased birth weight Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased birth weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased birth body size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased birth weight Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased birth weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

embryo development ending in birth or egg hatching Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2025 dataset.

alcohol-related birth defects Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease alcohol-related birth defects in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Abnormality of prenatal development or birth Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Abnormality of prenatal development or birth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Premature birth Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Premature birth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

spontaneous preterm birth x maternal stress interaction (1df) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the spontaneous preterm birth x maternal stress interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Age at first birth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Age at first birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Gestational age at birth (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gestational age at birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Spontaneous preterm birth (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Spontaneous preterm birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Birth length Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Birth length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Birth weight Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Spontaneous preterm birth (preterm delivery) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Spontaneous preterm birth (preterm delivery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Offspring birth weight Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Offspring birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Preterm birth (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Preterm birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

BMI at birth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the BMI at birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Moderate-to-late spontaneous preterm birth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Moderate-to-late spontaneous preterm birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Spontaneous preterm birth with premature rupture of membranes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Spontaneous preterm birth with premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Spontaneous preterm birth without premature rupture of membranes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Spontaneous preterm birth without premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Gestational age at birth (child effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gestational age at birth (child effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Early spontaneous preterm birth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Early spontaneous preterm birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Post-term birth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Post-term birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Birth weight variance Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Birth weight variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Ossification of the posterior longitudinal ligament of the spine Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ossification of the posterior longitudinal ligament of the spine from the curated CTD Gene-Disease Associations dataset.

Ossification, Heterotopic Gene Set

From CTD Gene-Disease Associations

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

ossification of the posterior longitudinal ligament of the spine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ossification of the posterior longitudinal ligament of the spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ossification of the posterior longitudinal ligament Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ossification of the posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ossification of the posterior longitudinal ligament of the spine (opll) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ossification of the posterior longitudinal ligament of the spine (opll) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ossification of spine Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; ossification of posterior longitudinal ligament Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ossification of posterior longitudinal ligament Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal ossification Gene Set

From GAD Gene-Disease Associations

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

ossification Gene Set

From GeneRIF Biological Term Annotations

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

ossification involved in bone remodeling Gene Set

From GO Biological Process Annotations 2015

genes participating in the ossification involved in bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset.

direct ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the direct ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

endochondral ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

replacement ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the replacement ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

ossification involved in bone maturation Gene Set

From GO Biological Process Annotations 2015

genes participating in the ossification involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.

intramembranous ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of ossification Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.

abnormal ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

absent sternal ossification Gene Set

From HPO Gene-Disease Associations

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

irregular ossification at anterior rib ends Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular ossification at anterior rib ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal enchondral ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal humeral ossification Gene Set

From HPO Gene-Disease Associations

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

decreased calvarial ossification Gene Set

From HPO Gene-Disease Associations

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

delayed tarsal ossification Gene Set

From HPO Gene-Disease Associations

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

cartilaginous ossification of larynx Gene Set

From HPO Gene-Disease Associations

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

multicentric ossification of proximal femoral epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multicentric ossification of proximal humeral epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the multicentric ossification of proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal tarsal ossification Gene Set

From HPO Gene-Disease Associations

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

ectopic ossification in ligament tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in ligament tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skull ossification Gene Set

From HPO Gene-Disease Associations

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

delayed patellar ossification Gene Set

From HPO Gene-Disease Associations

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

delayed femoral head ossification Gene Set

From HPO Gene-Disease Associations

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

absent in utero rib ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal metatarsal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal pelvis bone ossification Gene Set

From HPO Gene-Disease Associations

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

ectopic ossification in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ossification of the pubic bone Gene Set

From HPO Gene-Disease Associations

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

cartilaginous ossification of nose Gene Set

From HPO Gene-Disease Associations

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

delayed phalangeal epiphyseal ossification Gene Set

From HPO Gene-Disease Associations

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

irregular ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

abnormal ossification involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

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

abnormal epiphyseal ossification Gene Set

From HPO Gene-Disease Associations

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

delayed ossification of pubic rami Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed ossification of pubic rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

advanced tarsal ossification Gene Set

From HPO Gene-Disease Associations

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

delayed pubic bone ossification Gene Set

From HPO Gene-Disease Associations

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

increased skull ossification Gene Set

From HPO Gene-Disease Associations

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

irregular ossification of the humeral epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular ossification of the humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular tarsal ossification Gene Set

From HPO Gene-Disease Associations

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

ectopic ossification in tendon tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the ectopic ossification in tendon tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral ossification Gene Set

From HPO Gene-Disease Associations

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

absent in utero ossification of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone ossification Gene Set

From HPO Gene-Disease Associations

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

decreased skull ossification Gene Set

From HPO Gene-Disease Associations

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

delayed calcaneal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal foot bone ossification Gene Set

From HPO Gene-Disease Associations

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

decreased cranial base ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased cranial base ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hand bone ossification Gene Set

From HPO Gene-Disease Associations

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

multicentric femoral head ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the multicentric femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectopic ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal rib ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal sternal ossification Gene Set

From HPO Gene-Disease Associations

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

delayed epiphyseal ossification Gene Set

From HPO Gene-Disease Associations

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

Ossification of Posterior Longitudinal Ligament Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ossification of Posterior Longitudinal Ligament phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed bone ossification Gene Set

From MPO Gene-Phenotype Associations

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

failure of bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ossification involved in bone maturation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of sternum ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of sternum ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature bone ossification Gene Set

From MPO Gene-Phenotype Associations

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

abnormal long bone epiphyseal ossification zone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone ossification Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sternum ossification Gene Set

From MPO Gene-Phenotype Associations

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

impaired ossification of basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Endochondral Ossification(Homo sapiens) Gene Set

From WikiPathways Pathways 2014

proteins participating in the Endochondral Ossification(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

Endochondral Ossification(Mus musculus) Gene Set

From WikiPathways Pathways 2014

proteins participating in the Endochondral Ossification(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

Ectopic Ossification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ectopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Bone Ossification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ossification Of The Posterior Longitudinal Ligament Of Spine Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ossification Of The Posterior Longitudinal Ligament Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Absent Ossification Of Calvaria Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Absent Ossification Of Calvaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Enchondral Ossification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Enchondral Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Pelvis Bone Ossification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Pelvis Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Foot Bone Ossification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Foot Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ectopic Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ectopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Calvarial Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Calvarial Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Proximal Femoral Epiphyseal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent In Utero Ossification Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent In Utero Ossification Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent In Utero Rib Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent In Utero Rib Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Heterotopic Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Heterotopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Advanced Tarsal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Advanced Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Epiphyseal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Cranial Base Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Cranial Base Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Calcaneal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Calcaneal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Pubic Bone Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Pubic Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Sternal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Sternal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Early Ossification Of Capital Femoral Epiphyses Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Early Ossification Of Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Epiphyseal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Irregular Ossification At Anterior Rib Ends Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregular Ossification At Anterior Rib Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Femoral Head Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multicentric Femoral Head Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multicentric Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multicentric Ossification Of Proximal Femoral Epiphyses Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multicentric Ossification Of Proximal Humeral Epiphyses Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multicentric Ossification Of Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Irregular Tarsal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregular Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Incomplete Ossification Of Pubis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Incomplete Ossification Of Pubis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Sternal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Sternal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Hand Bone Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Hand Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Ossification Involving The Femoral Head And Neck Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Ossification Involving The Femoral Head And Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Ossification Of Pubic Rami Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Ossification Of Pubic Rami in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Tarsal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Patellar Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Patellar Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Delayed Phalangeal Epiphyseal Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Delayed Phalangeal Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cartilaginous Ossification Of Larynx Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cartilaginous Ossification Of Larynx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cartilaginous Ossification Of Nose Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cartilaginous Ossification Of Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Irregular Ossification Of Hand Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregular Ossification Of Hand Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

endochondral ossification Gene Set

From GO Biological Process Annotations 2023

genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of ossification Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of ossification Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of ossification Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.

intramembranous ossification Gene Set

From GO Biological Process Annotations 2023

genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2023 dataset.

abnormal sternum ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal sternum ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal long bone epiphyseal ossification zone morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

impaired ossification of basisphenoid bone Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

delayed endochondral bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal endochondral bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

delayed bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intramembranous bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

delayed intramembranous bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

premature bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the premature bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

failure of bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the failure of bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

premature endochondral bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

premature intramembranous bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

failure of sternum ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the failure of sternum ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

failure of endochondral bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the failure of endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

failure of intramembranous bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the failure of intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal palatal shelf bone ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal palatal shelf bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal ossification involved in bone maturation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal perichondrial ossification Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal perichondrial ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Endochondral ossification Gene Set

From WikiPathways Pathways 2024

proteins participating in the Endochondral ossification pathway from the WikiPathways Pathways 2024 dataset.

Endochondral ossification with skeletal dysplasias Gene Set

From WikiPathways Pathways 2024

proteins participating in the Endochondral ossification with skeletal dysplasias pathway from the WikiPathways Pathways 2024 dataset.

endochondral ossification Gene Set

From GO Biological Process Annotations 2025

genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of ossification Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of ossification Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of ossification Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.

intramembranous ossification Gene Set

From GO Biological Process Annotations 2025

genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2025 dataset.

Ossification of the posterior longitudinal ligament of spine Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Ossification of the posterior longitudinal ligament of spine in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Ossification of the posterior longitudinal ligament of spine Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ossification of the posterior longitudinal ligament of spine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ossification of the posterior longitudinal ligament of the spine Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Ossification of the posterior longitudinal ligament of the spine phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.