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abnormality of the thoracic spine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thoracic spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Thoracic Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Thoracic Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
thoracic spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thoracic spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Thoracic spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thoracic spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lumbar spine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lumbar spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Cervical Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Cervical Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Lumbar Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Lumbar Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormality of the thoracic cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thoracic cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Brachyrachia (short spine dysplasia) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
neuron spine Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuron spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dendritic spine neck Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dendritic spine neck cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
axonal spine Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the axonal spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dendritic spine membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dendritic spine membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dendritic spine Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dendritic spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dendritic spine head Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dendritic spine head cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
neuron spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the neuron spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
spine mat Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spine mat cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dendritic spine neck Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dendritic spine neck cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
spine apparatus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spine apparatus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
somatic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the somatic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
axonal spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the axonal spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dendritic spine membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dendritic spine membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dendritic spine head Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dendritic spine head cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dendritic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dendritic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Ossification of the posterior longitudinal ligament of the spine Gene SetFrom 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. |
Rigid spine syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rigid spine syndrome from the curated CTD Gene-Disease Associations dataset. |
ossification of the posterior longitudinal ligament of the spine Gene SetFrom 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. |
early postmenopausal bone loss at the spine. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early postmenopausal bone loss at the spine. 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 SetFrom 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 SetFrom 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. |
bone mineral density (spine) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density (spine) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disc degeneration, lumbar spine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disc degeneration, lumbar spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spine Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term spine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
negative regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset. |
dendritic spine development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2015 dataset. |
dendritic spine organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dendritic spine organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset. |
neuron spine Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the neuron spine cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
dendritic spine neck Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the dendritic spine neck cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
axonal spine Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the axonal spine cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
dendritic spine membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the dendritic spine membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
dendritic spine Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the dendritic spine cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
dendritic spine head Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the dendritic spine head cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Spine bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Spine bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Bone mineral density (spine) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
relatively short spine Gene SetFrom HPO Gene-Disease Associations genes associated with the relatively short spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormally straight spine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormally straight spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased cervical spine mobility Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cervical spine Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive cervical vertebral spine fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cervical spine hypermobility Gene SetFrom HPO Gene-Disease Associations genes associated with the cervical spine hypermobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Osteoarthritis, Spine Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Osteoarthritis, Spine phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal scapular spine morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scapular spine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dendritic spine morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dendritic spine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spine curvature Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spine curvature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscular dystrophy, rigid spine, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cervical spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cervical spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ischial spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ischial spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
lumbar spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue lumbar spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Deformity Of Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deformity Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Kyphoscoliosis Deformity Of Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Kyphoscoliosis Deformity Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Degeneration Of Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ossification Of The Posterior Longitudinal Ligament Of Spine Gene SetFrom 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. |
Other Congenital Malformations Of Spine, Not Associated With Scoliosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Spine, Not Associated With Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Spine Instability Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spine Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spine Stiffness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spine Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Relatively Short Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Relatively Short Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lumbar Spine Degeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lumbar Spine Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Kyphosis Deformity Of Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Kyphosis Deformity Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Cervical Vertebral Spine Fusion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Cervical Vertebral Spine Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cervical Spine Mobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cervical Spine Hypermobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Spine Hypermobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormally Straight Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormally Straight Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Curvature Of Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Curvature Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
positive regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2023 dataset. |
dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
dendritic spine organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the dendritic spine organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
multiple spine synapse organization, single dendrite Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2023 dataset. |
modification of dendritic spine Gene SetFrom GO Biological Process Annotations 2023 genes participating in the modification of dendritic spine biological process from the curated GO Biological Process Annotations 2023 dataset. |
spine apparatus assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the spine apparatus assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
multiple spine synapse organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
dendritic spine membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the dendritic spine membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
neuron spine Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the neuron spine cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal spine curvature Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spine curvature phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal scapular spine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal scapular spine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic spine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic spine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased dendritic spine density Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased dendritic spine density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased dendritic spine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased dendritic spine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased dendritic spine number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased dendritic spine number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased dendritic spine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased dendritic spine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased dendritic spine number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased dendritic spine number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased dendritic spine density Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased dendritic spine density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic mushroom spine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic mushroom spine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic stubby spine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic stubby spine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic spine density Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic spine density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dendritic thin spine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendritic thin spine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal spine curvature Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal spine curvature phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
spine apparatus Gene SetFrom SynGO Synaptic Gene Annotations genes associated with the synaptic term spine apparatus from the SynGO Synaptic Gene Annotations dataset. |
integral component of spine apparatus membrane Gene SetFrom SynGO Synaptic Gene Annotations genes associated with the synaptic term integral component of spine apparatus membrane from the SynGO Synaptic Gene Annotations dataset. |
positive regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2025 dataset. |
dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of dendritic spine development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of dendritic spine maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of dendritic spine maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of dendritic spine morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of dendritic spine morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
dendritic spine organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the dendritic spine organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
multiple spine synapse organization, single dendrite Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2025 dataset. |
spine apparatus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spine apparatus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
multiple spine synapse organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
dendritic spine membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the dendritic spine membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
neuron spine Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the neuron spine cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Ossification of the posterior longitudinal ligament of spine Gene SetFrom 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 SetFrom 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. |
Rigid spine muscular dystrophy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rigid spine muscular dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lumbar spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Lumbar spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cervical spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cervical spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ischial spine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ischial spine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Neuron spine Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuron spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Dendritic spine cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine head Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Dendritic spine head cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Dendritic spine membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Spine apparatus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Spine apparatus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Neuron spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuron spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spine apparatus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spine apparatus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spine synapse Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spine synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine neck Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine neck cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine head Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine head cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Somatic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Somatic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spine mat Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spine mat cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Axonal spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonal spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Actin cytoskeleton of dendritic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Actin cytoskeleton of dendritic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cytoskeleton of dendritic spine Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytoskeleton of dendritic spine cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cytoplasmic side of dendritic spine plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytoplasmic side of dendritic spine plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Spine apparatus membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Spine apparatus membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine cytoplasm Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine cytoplasm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dendritic spine origin Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dendritic spine origin cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Juvenile osteochondrosis of spine Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile osteochondrosis of spine phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bone mineral density (spine) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (spine) and age at menarche Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (spine) and age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low bone mineral density (spine) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spine bone mineral density and alcohol drinking Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spine bone mineral density and alcohol drinking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral density (spine) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral content (spine) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral content (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lumbar spine bone mineral density (trabecular) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lumbar spine bone mineral density (trabecular) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lumbar spine bone mineral density (integral) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lumbar spine bone mineral density (integral) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Ossification of the posterior longitudinal ligament of the spine Gene SetFrom 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. |
Spine bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spine bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lumbar spine bone mineral density Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lumbar spine bone mineral density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (lumbar spine) in inflammatory bowel disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (lumbar spine) in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic aneurysm, familial thoracic 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Asphyxiating thoracic dystrophy 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Asphyxiating thoracic dystrophy 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Asphyxiating thoracic dystrophy 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 11 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 10 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 3 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thoracic Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thoracic Diseases from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Thoracic from the curated CTD Gene-Disease Associations dataset. |
Asphyxiating Thoracic Dystrophy 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset. |
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Thoracic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
thoracic cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease thoracic cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
asphyxiating thoracic dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
thoracic cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease thoracic cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
thoracic benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic outlet syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic outlet syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
asphyxiating thoracic dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, thoracic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, thoracic; aortic rupture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic; aortic rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thoracic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term thoracic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
thoracic cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease thoracic cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
thoracic aortic aneurysm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease thoracic aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
anterior beaking of thoracic vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior beaking of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bifid thoracic vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the bifid thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior beaking of lower thoracic vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior beaking of lower thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dilatation of the descending thoracic aorta Gene SetFrom HPO Gene-Disease Associations genes associated with the dilatation of the descending thoracic aorta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic hemivertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic hemivertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lower thoracic interpediculate narrowness Gene SetFrom HPO Gene-Disease Associations genes associated with the lower thoracic interpediculate narrowness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic platyspondyly Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic platyspondyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lower thoracic kyphosis Gene SetFrom HPO Gene-Disease Associations genes associated with the lower thoracic kyphosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic kyphosis Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic kyphosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic scoliosis Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior concavity of thoracic vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior concavity of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Thoracic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Thoracic Injuries Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Thoracic Injuries phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Thoracic Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Thoracic Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal thoracic aorta morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic aorta morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal descending thoracic aorta morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal descending thoracic aorta morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic cage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic cage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thoracic vertebral fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased thoracic vertebrae number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged thoracic cavity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged thoracic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thoracic cage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thoracic cage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thoracic cavity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thoracic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic vertebrae morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic vertebrae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic cage shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic cage shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thoracic vertebral transformation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thoracic aorta aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thoracic aorta aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
calcified thoracic aorta Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the calcified thoracic aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased thoracic vertebrae number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short-rib thoracic dysplasia 10 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 4 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 6 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 7 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 11 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 9 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 3 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 8 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 2 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 5 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
thoracic leg Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thoracic leg in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
thoracic ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thoracic ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Dilation Of The Thoracic Aorta Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dilation Of The Thoracic Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dissecting Aneurysm Of The Thoracic Aorta Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Aneurysm Of The Thoracic Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Thoracic Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Thoracic Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Aortic Ectasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Aortic Ectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Jeune Thoracic Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Jeune Thoracic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short-Rib Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Descending Thoracic Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Descending Thoracic Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fused Thoracic Vertebrae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fused Thoracic Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Outlet Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Outlet Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anterior Beaking Of Thoracic Vertebrae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anterior Beaking Of Thoracic Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anterior Beaking Of Lower Thoracic Vertebrae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anterior Beaking Of Lower Thoracic Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Discitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Discitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Myelopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Hemivertebra Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Hemivertebra in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Scoliosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thoracic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thoracic Kyphoscoliosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thoracic Kyphoscoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thoracic Kyphosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thoracic Kyphosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prolapsed Thoracic Intervertebral Disc Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolapsed Thoracic Intervertebral Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Concavity Of Thoracic Vertebrae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Concavity Of Thoracic Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thoracic Platyspondyly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thoracic Platyspondyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thoracic Aorta Calcification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thoracic Aorta Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lower Thoracic Interpediculate Narrowness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Thoracic Interpediculate Narrowness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short-Rib Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lower Thoracic Kyphosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Thoracic Kyphosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bifid Thoracic Vertebrae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifid Thoracic Vertebrae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cerebro-Facio-Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebro-Facio-Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal thoracic cage morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic cage morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic cavity morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic cavity morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic vertebrae morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic vertebrae morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thoracic vertebral transformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small thoracic cavity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small thoracic cavity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged thoracic cavity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged thoracic cavity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small thoracic cage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small thoracic cage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased thoracic vertebrae number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased thoracic vertebrae number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal descending thoracic aorta morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal descending thoracic aorta morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic cage shape Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic cage shape phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thoracic vertebral fusion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased thoracic vertebrae number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased thoracic vertebrae number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic aorta morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic aorta morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic mammary gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic mammary gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thoracic aorta aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thoracic aorta aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
calcified thoracic aorta Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified thoracic aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic cage shape Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal thoracic cage shape phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Thoracic thymus_CT1_thymic capsular fibroblast Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_thymic capsular fibroblast cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_macrophage Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_macrophage cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_sympathetic noradrenergic nerve Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_sympathetic noradrenergic nerve cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_blood endothelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_blood endothelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_thymic interlobular fibroblast Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_thymic interlobular fibroblast cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_erythroid Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_erythroid cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_mast cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_mast cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_eosinophil Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_eosinophil cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_early thymic progenitor Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_early thymic progenitor cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_double negative thymocyte 2 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 2 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_double negative thymocyte 3 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 3 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_double negative thymocyte 4 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 4 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_double positive thymocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_double positive thymocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_plasmacytoid dendritic cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_plasmacytoid dendritic cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_cortical thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_cortical thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_memory B cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_memory B cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_plasmablast Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_plasmablast cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_plasma cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_plasma cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_monocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_monocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD4+ T single positive thymocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD4+ T single positive thymocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD8+ T single positive thymocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD8+ T single positive thymocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_conventional dendritic cell 1 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_conventional dendritic cell 1 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_conventional dendritic cell 2 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_conventional dendritic cell 2 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_lymphatic endothelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_lymphatic endothelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_corticomedullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_corticomedullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_cytotoxic CD4 T cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_cytotoxic CD4 T cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD4+ T memory T cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD4+ T memory T cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD8+ T memory Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD8+ T memory cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD8aa(I) thymocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD8aa(I) thymocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD8aa(II) thymocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_CD8aa(II) thymocyte cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_T follicular helper cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_T follicular helper cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_regulatory T cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_regulatory T cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_gamma-delta T cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_gamma-delta T cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_Th17 cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_Th17 cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_mucosal associated invariant T cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_mucosal associated invariant T cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_immature NKT cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_immature NKT cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_naive B cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_naive B cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_group 3 innate lymphoid cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_group 3 innate lymphoid cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_natural killer cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_natural killer cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 1 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 1 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 2 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 2 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 3 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 3 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 4 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 4 cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_CD4+ T memory T cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD4+ T memory T cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_CD4+ T single positive thymocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD4+ T single positive thymocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_CD8+ T memory Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD8+ T memory cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_CD8+ T single positive thymocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD8+ T single positive thymocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_CD8aa(I) thymocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD8aa(I) thymocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_CD8aa(II) thymocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_CD8aa(II) thymocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_T follicular helper cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_T follicular helper cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_Th17 cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_Th17 cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_blood endothelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_blood endothelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_conventional dendritic cell 1 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_conventional dendritic cell 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_conventional dendritic cell 2 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_conventional dendritic cell 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_cortical thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_cortical thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_corticomedullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_corticomedullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_cytotoxic CD4 T cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_cytotoxic CD4 T cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_double negative thymocyte 2 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_double negative thymocyte 3 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_double negative thymocyte 4 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_double negative thymocyte 4 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_double positive thymocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_double positive thymocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_early thymic progenitor Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_early thymic progenitor cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_eosinophil Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_eosinophil cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_erythroid Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_erythroid cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_gamma-delta T cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_gamma-delta T cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_group 3 innate lymphoid cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_group 3 innate lymphoid cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_immature NKT cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_immature NKT cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_lymphatic endothelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_lymphatic endothelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_macrophage Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_macrophage cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_mast cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_mast cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 1 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 2 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 3 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_medullary thymic epithelial cell type 4 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_medullary thymic epithelial cell type 4 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_memory B cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_memory B cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_monocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_monocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_mucosal associated invariant T cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_mucosal associated invariant T cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_naive B cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_naive B cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_natural killer cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_natural killer cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_plasma cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_plasma cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_plasmablast Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_plasmablast cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_plasmacytoid dendritic cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_plasmacytoid dendritic cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_regulatory T cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_regulatory T cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_sympathetic noradrenergic nerve Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_sympathetic noradrenergic nerve cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_thymic capsular fibroblast Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_thymic capsular fibroblast cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_thymic interlobular fibroblast Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_thymic interlobular fibroblast cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thoracic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 9 with or without polydactyly Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease short-rib thoracic dysplasia 9 with or without polydactyly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thoracic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 9 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 9 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 6 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 6 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 10 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 10 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic outlet syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic outlet syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 14 with polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 14 with polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 8 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 8 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 11 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 11 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 13 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 13 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
short-rib thoracic dysplasia 7 with or without polydactyly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 7 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Asphyxiating thoracic dystrophy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asphyxiating thoracic dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thoracic ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Thoracic leg Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thoracic leg in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Familial thoracic aortic aneurysm and aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial thoracic aortic aneurysm and aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysm or dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm or dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short-rib thoracic dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short-rib thoracic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Asphyxiating thoracic dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Asphyxiating thoracic dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Jeune thoracic dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Jeune thoracic dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Isolated thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heritable Thoracic Aortic disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heritable Thoracic Aortic disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early age onset of sporadic thoracic aortic dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebro-facio-thoracic dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebro-facio-thoracic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic-to-hip circumference ratio Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic-to-hip circumference ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic calcification levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Congenital heart disease (anomalies of thoracic arteries and veins) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital heart disease (anomalies of thoracic arteries and veins) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness 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 SetFrom 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. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom 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. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom 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. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom 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. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ganglioside metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of humoral immunity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sixth cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calvarial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine bicarbonate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genitourinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fascia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the liver Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental color Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alkaline phosphatase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the larynx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the salivary glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacroiliac joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lacrimal duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corticospinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the endocrine system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the endocrine system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the soft palate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the adrenal glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the adrenal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the periorbital region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the periorbital region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the respiratory system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fontanelles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the septum pellucidum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renal excretion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renal excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the premaxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eeg abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the eeg abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renin-angiotensin system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
c1-c2 vertebral abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pectoral muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pectoral muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of descemet's membrane Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of descemet's membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sclera Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sclera phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
phenotypic abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the phenotypic abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating adrenocorticotropin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating adrenocorticotropin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radial head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radial head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasolabial region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasolabial region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the uvea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of female external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of tyrosine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of tyrosine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of extrapyramidal motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the rectum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the rectum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |