Decreased central vision

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Results for "Decreased central vision": 1001 gene sets

Name
decreased central vision Gene Set From HPO Gene-Disease Associations genes associated with the decreased central vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central nervous system neoplasms; central nervous system tumors; glioma Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Vision Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vision Disorders from the curated CTD Gene-Disease Associations dataset.
Color Vision Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Color Vision Defects from the curated CTD Gene-Disease Associations dataset.
Vision, Low Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vision, Low from the curated CTD Gene-Disease Associations dataset.
binocular vision disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease binocular vision disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
defective colour vision Gene Set From GAD Gene-Disease Associations genes associated with the disease defective colour vision in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glaucoma, open-angle; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
color vision defects; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; corneal diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; corneal diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal diseases; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vision Gene Set From GAD High Level Gene-Disease Associations genes associated with the disease vision in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
vision Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term vision in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
abnormality of vision Gene Set From 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 binocular vision Gene Set From 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 vision evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of color vision Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of color vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
blurred vision Gene Set From HPO Gene-Disease Associations genes associated with the blurred vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hemianopic blurring of vision Gene Set From HPO Gene-Disease Associations genes associated with the hemianopic blurring of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Vision Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vision phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vision Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vision Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mesopic Vision Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mesopic Vision phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Color Vision Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Color Vision phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Color Vision Defects Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Color Vision Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vision, Low Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vision, Low phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal vision Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vision phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vision/eye phenotype Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
The canonical retinoid cycle in rods (twilight vision) Gene Set From Reactome Pathways 2014 proteins participating in the The canonical retinoid cycle in rods (twilight vision) pathway from the Reactome Pathways dataset.
The retinoid cycle in cones (daylight vision) Gene Set From Reactome Pathways 2014 proteins participating in the The retinoid cycle in cones (daylight vision) pathway from the Reactome Pathways dataset.
Abnormality Of Vision Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Low Vision Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Low Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vision Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vision Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vision Impairment And Blindness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vision Impairment And Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Blurred Vision Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blurred Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Blurred Vision, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blurred Vision, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Vision Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Color Vision Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Color Vision Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Unilateral Blurring Of Vision Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Unilateral Blurring Of Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Color Vision Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Color Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Color Vision Test Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Color Vision Test Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal vision Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vision phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vision/eye phenotype Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
The canonical retinoid cycle in rods (twilight vision) Gene Set From Reactome Pathways 2024 proteins participating in the The canonical retinoid cycle in rods (twilight vision) pathway from the Reactome Pathways 2024 dataset.
The retinoid cycle in cones (daylight vision) Gene Set From Reactome Pathways 2024 proteins participating in the The retinoid cycle in cones (daylight vision) pathway from the Reactome Pathways 2024 dataset.
Binocular vision disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Binocular vision disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Color vision defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Color vision defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Blurred vision Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Blurred vision phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormality of vision Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of vision phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Computer vision syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Computer vision syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
decreased central memory CD4-positive, alpha-beta T cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased central memory CD8 positive, alpha-beta T cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
central medullary reticular group, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
precentral gyrus, right, bank of the central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in precentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
postcentral gyrus, left, bank of the posterior central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, left, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central nucleus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central gray substance of midbrain, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
precentral gyrus, left, bank of the central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in precentral gyrus, left, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central gray of the pons, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray of the pons, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central gray of the pons, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray of the pons, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central glial substance Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central glial substance relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
postcentral gyrus, left, bank of the central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, left, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central gray substance of midbrain, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central medullary reticular group, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
postcentral gyrus, right, bank of the central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
postcentral gyrus, right, bank of the posterior central sulcus Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, right, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central part of MPO Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of MPO relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central amygdaloid nucleus, medial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central amygdaloid nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central part of MD Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of MD relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central subpallium (classic basal ganglia) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central subpallium (classic basal ganglia) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterior hypothalamic nucleus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Pontine central gray Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pontine central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r4 liminal central gray Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r4 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central amygdalar nucleus, medial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central lobule Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central lobule relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central lateral nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central lateral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central amygdalar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central amygdalar nucleus, capsular part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, capsular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central part of VMH Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of VMH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Ventromedial hypothalamic nucleus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior central nucleus raphe, lateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior central nucleus raphe, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central amygdalar nucleus, lateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central nucleus of the inferior colliculus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus of the inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Inferior colliculus, central nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Inferior colliculus, central nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central lateral nucleus of the thalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central lateral nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior central nucleus raphe Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior central nucleus raphe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central medial nucleus of the thalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central medial nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Parabrachial nucleus, lateral division, central lateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Parabrachial nucleus, lateral division, central lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Mediodorsal nucleus of the thalamus, central part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Mediodorsal nucleus of the thalamus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r2 liminal central gray Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r2 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r3 liminal central gray Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r3 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central layers of TG Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central layers of TG relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
nucleus of the central acoustic tract Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the central acoustic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Central linear nucleus raphe Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central linear nucleus raphe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
central portion of GPi Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central portion of GPi relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
central part of CEl Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central part of CEl relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
central nucleus of inferior colliculus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
central nuclear group Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nuclear group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
medial subdivision of central nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in medial subdivision of central nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Central precocious puberty Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Central core disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Single upper central incisor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
central element Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the central element cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nuclear pore central transport channel Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
central element Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the central element cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
central vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the central vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Central Nervous System Agents Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Central Nervous System Agents from the curated CTD Gene-Chemical Interactions dataset.
Cataract, Central Saccular, With Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Central Saccular, With Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Myopathy, Central Core Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Central Core from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Central Nervous System Infections Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Infections from the curated CTD Gene-Disease Associations dataset.
Vasculitis, Central Nervous System Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vasculitis, Central Nervous System from the curated CTD Gene-Disease Associations dataset.
Congenital central hypoventilation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.
Central Nervous System Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Diseases from the curated CTD Gene-Disease Associations dataset.
Precocious Puberty, Central Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Precocious Puberty, Central from the curated CTD Gene-Disease Associations dataset.
Central Nervous System Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Neoplasms from the curated CTD Gene-Disease Associations dataset.
Choroidal dystrophy central areolar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.
Hemangioma, Cavernous, Central Nervous System Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemangioma, Cavernous, Central Nervous System from the curated CTD Gene-Disease Associations dataset.
Single upper central incisor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Single upper central incisor from the curated CTD Gene-Disease Associations dataset.
Central Nervous System Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Central Nervous System in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
central nervous system disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central nervous system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
autoimmune disease of central nervous system Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central core myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
central nervous system disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease central nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
central nervous system cancer Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease central nervous system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
central nervous system lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system tuberculosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central core myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system origin vertigo Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system origin vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central epithelioid sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system hereditary degenerative disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system hereditary degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central pontine myelinolysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system germinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system mesenchymal non-meningothelial tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune disease of central nervous system Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
conventional central osteosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conventional central osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system primitive neuroectodermal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system primitive neuroectodermal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central neurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central neurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system melanocytic neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system melanocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hearing loss, central Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital central hypoventilation syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital central hypoventilation syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
loperamide disposition and central nervous system effects. Gene Set From GAD Gene-Disease Associations genes associated with the disease loperamide disposition and central nervous system effects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system neoplasms; lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus vasculitis, central nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus vasculitis, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain neoplasms; hemangioma, cavernous, central nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; hemangioma, cavernous, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; central nervous system vascular malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; central nervous system vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus nephritis; lupus vasculitis, central nervous system; nephritis sle Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus nephritis; lupus vasculitis, central nervous system; nephritis sle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggression, impulsivity, and central nervous system serotonergic responsivity Gene Set From GAD Gene-Disease Associations genes associated with the disease aggression, impulsivity, and central nervous system serotonergic responsivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central adiposity Gene Set From GAD Gene-Disease Associations genes associated with the disease central adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central core disease Gene Set From GAD Gene-Disease Associations genes associated with the disease central core disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system diseases; hiv infections Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system diseases; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central pulse pressure Gene Set From GAD Gene-Disease Associations genes associated with the disease central pulse pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercapnic respiratory failure; hypoventilation; sleep apnea, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central nervous system relapse Gene Set From GAD Gene-Disease Associations genes associated with the disease central nervous system relapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
central Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term central in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
central nervous system interneuron axonogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system interneuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system myelination Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system vasculogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system myelin maintenance Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of central b cell tolerance induction Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of central b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system myelin formation Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system neuron development Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of central tolerance induction Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system development Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of central b cell tolerance induction Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of central b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
central tolerance induction Gene Set From GO Biological Process Annotations 2015 genes participating in the central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system projection neuron axonogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
axon ensheathment in central nervous system Gene Set From GO Biological Process Annotations 2015 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of central tolerance induction Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
central nervous system neuron axonogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
central element Gene Set From GO Cellular Component Annotations 2015 proteins localized to the central element cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Central corneal thickness Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
central nervous system disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease central nervous system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
central nervous system cancer Gene Set From GWASdb SNP-Disease Associations genes associated with the disease central nervous system cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
neoplasm of the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of central motor function Gene Set From 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 central nervous system electrophysiology Gene Set From 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.
aplasia/hypoplasia involving the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
malignant neoplasm of the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the malignant neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
morphological abnormality of the central nervous system Gene Set From 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.
atrophy/degeneration affecting the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
benign neoplasm of the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the benign neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
central hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the central hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of central somatosensory evoked potentials Gene Set From 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.
malignant neoplasm of the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the malignant neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal central microtubular pair morphology of respiratory motile cilia Gene Set From HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central scotoma Gene Set From HPO Gene-Disease Associations genes associated with the central scotoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
morphological abnormality of the central nervous system Gene Set From 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.
central hypothyroidism Gene Set From HPO Gene-Disease Associations genes associated with the central hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
benign neoplasm of the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the benign neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysplastic distal thumb phalanges with a central hole Gene Set From HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of central nervous system electrophysiology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of central nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lipomas of the central neryous system Gene Set From HPO Gene-Disease Associations genes associated with the lipomas of the central neryous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of central motor function Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of central motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sudden central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central apnea Gene Set From HPO Gene-Disease Associations genes associated with the central apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
agenesis of central incisor Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
widely-spaced maxillary central incisors Gene Set From HPO Gene-Disease Associations genes associated with the widely-spaced maxillary central incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central opacification of the cornea Gene Set From HPO Gene-Disease Associations genes associated with the central opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central diabetes insipidus Gene Set From HPO Gene-Disease Associations genes associated with the central diabetes insipidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
agenesis of mandibular central incisor Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of mandibular central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central adrenal insufficiency Gene Set From HPO Gene-Disease Associations genes associated with the central adrenal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macrodontia of permanent maxillary central incisor Gene Set From HPO Gene-Disease Associations genes associated with the macrodontia of permanent maxillary central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neuronal loss in central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline central nervous system lipomas Gene Set From HPO Gene-Disease Associations genes associated with the midline central nervous system lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene Set From HPO Gene-Disease Associations genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central hypoventilation Gene Set From HPO Gene-Disease Associations genes associated with the central hypoventilation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central nervous system degeneration Gene Set From HPO Gene-Disease Associations genes associated with the central nervous system degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neoplasm of the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large central visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Central Serous Chorioretinopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Central Serous Chorioretinopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Central Nervous System Vascular Malformations Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Vascular Malformations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hearing Loss, Central Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vasculitis, Central Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vasculitis, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea, Central Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Central Nervous System Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Central Nervous System Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hemangioma, Cavernous, Central Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hemangioma, Cavernous, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hereditary Central Nervous System Demyelinating Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Central Nervous System Demyelinating Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lupus Vasculitis, Central Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lupus Vasculitis, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
S-adenosylmethionine synthetase, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the S-adenosylmethionine synthetase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA topoisomerase, type IA, central region, subdomain 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA topoisomerase, type IA, central region, subdomain 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
MDM2-binding protein, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the MDM2-binding protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Ribosomal protein S4e, central region Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S4e, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Poly(A) polymerase, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Poly(A) polymerase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA topoisomerase, type IIA, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IIA, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synaptonemal complex central element protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex central element protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA topoisomerase, type IA, central Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Talin, central Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Talin, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA oxidase/dehydrogenase, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA oxidase/dehydrogenase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pro-opiomelanocortin/corticotropin, ACTH, central region Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pro-opiomelanocortin/corticotropin, ACTH, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.
TPX2 central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the TPX2 central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine pyrophosphate enzyme, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synaptonemal complex central element protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex central element protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
FERM central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FERM central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Hermansky-Pudlak syndrome 3, central region Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Hermansky-Pudlak syndrome 3, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sec16, central conserved domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sec16, central conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Interleukin-12 beta, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Interleukin-12 beta, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Runx, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Runx, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein-arginine deiminase (PAD), central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-arginine deiminase (PAD), central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mur ligase, central Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mur ligase, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glycoside hydrolase, family 65, central catalytic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 65, central catalytic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
DNA ligase, ATP-dependent, central Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA ligase, ATP-dependent, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vacuolar protein sorting-associated protein 8, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
RPA-interacting protein, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Developmental pluripotency-associated protein 2/4, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glycoside hydrolase, family 38, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
WASH complex subunit 7, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the WASH complex subunit 7, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Elongation factor 1 beta central acidic region, eukaryote Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Elongation factor 1 beta central acidic region, eukaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dynamin central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynamin central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glycoside hydrolase, families 57/38, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, families 57/38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Transcription elongation factor S-II, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription elongation factor S-II, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cactin, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cactin, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acetyl-CoA carboxylase, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-CoA carboxylase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cell morphogenesis central region Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell morphogenesis central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal central pattern generator function Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal central tendon morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal central tendon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord central canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal central nervous system regeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal central nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal central medial nucleus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal central medial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
precocious puberty, central, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the precocious puberty, central, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
single median maxillary central incisor Gene Set From OMIM Gene-Disease Associations genes associated with the single median maxillary central incisor phenotype from the curated OMIM Gene-Disease Associations dataset.
optic nerve hypoplasia and abnormalities of the central nervous system Gene Set From OMIM Gene-Disease Associations genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy with central cone involvement Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
choriodal dystrophy, central areolar 2 Gene Set From OMIM Gene-Disease Associations genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{efavirenz central nervous system toxicity, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {efavirenz central nervous system toxicity, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
hypothyroidism, central, and testicular enlargement Gene Set From OMIM Gene-Disease Associations genes associated with the hypothyroidism, central, and testicular enlargement phenotype from the curated OMIM Gene-Disease Associations dataset.
central core disease Gene Set From OMIM Gene-Disease Associations genes associated with the central core disease phenotype from the curated OMIM Gene-Disease Associations dataset.
?precocious puberty, central, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?precocious puberty, central, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
central nervous system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue central nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
central nervous system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue central nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
central amygdaloid nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
central nervous system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
midbrain central gray Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue midbrain central gray in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
central medial thalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central medial thalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Central Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Neuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Depression (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Depression (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Central Nervous System Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Central Nervous System Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Serous Chorioretinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Core Myopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Core Myopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ataxia With Central Nervous System Hypomyelinization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Demyelination Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Central Serous Chorioretinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Odontogenic Fibroma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Odontogenic Fibroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Metabolic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Metabolic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metabolic Disorder, Central Nervous System, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Disorder, Central Nervous System, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Lesion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Blindness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Central Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Solitary Median Maxillary Central Incisor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Solitary Median Maxillary Central Incisor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Hodgkin'S Lymphoma Of Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Angiitis Of The Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Angiitis Of The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Demyelinating Disease Of Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Demyelinating Disease Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Central Serous Chorioretinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Central Hypoventilation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Leukaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Leukaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Central Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Neurocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Neurocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Neoplasms, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Neoplasms, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Processing Disorder, Central Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Processing Disorder, Central in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Large B-Cell Lymphoma Of Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Sensitization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Sensitization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Neuropathic Pain Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Central Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Candidiasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lupus Vasculitis, Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lupus Vasculitis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cavernous Angioma, Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cavernous Angioma, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Embryonal Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Embryonal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Embryonal Tumor, Not Otherwise Specified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Embryonal Tumor, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Germinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Germinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Areolar Choroidal Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Areolar Choroidal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Low Grade Central Osteosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Central Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Melanocytic Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Melanocytic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculitis, Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculitis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion - Juvenile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion - Juvenile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Pain Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysplastic Distal Thumb Phalanges With A Central Hole Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toxoplasmosis, Central Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toxoplasmosis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Centrifugal Cicatricial Alopecia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Centrifugal Cicatricial Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Core Disease, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Core Disease, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Langerhans Cell Histiocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Topographic Island Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Topographic Island in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Central Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midline Central Nervous System Lipomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midline Central Nervous System Lipomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Nervous System Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Corneal Thickness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Corneal Thickness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuronal Loss In Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Post-Stroke Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Post-Stroke Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Heterochromia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Heterochromia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Widely-Spaced Maxillary Central Incisors Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widely-Spaced Maxillary Central Incisors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Hypoventilation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Retinal Vessel Vascular Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Retinal Vessel Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Y-Shaped Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Y-Shaped Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Opacification Of The Cornea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Opacification Of The Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Central Somatosensory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Vertebral Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Vertebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Central Focal Spikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Central Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Cyanosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Cyanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Large Central Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Core Regions In Muscle Fibers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Core Regions In Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Central Sensory Function Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Sensory Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Central Motor Conduction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Motor Conduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
central nervous system development Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system neuron axonogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system myelination Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2023 dataset.
central tolerance induction to self antigen Gene Set From GO Biological Process Annotations 2023 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system projection neuron axonogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system neuron development Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system myelin maintenance Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system vasculogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
axonemal central apparatus assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
central nervous system myelin formation Gene Set From GO Biological Process Annotations 2023 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of central B cell tolerance induction Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
axon ensheathment in central nervous system Gene Set From GO Biological Process Annotations 2023 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of central tolerance induction Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of central B cell tolerance induction Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal spinal cord central canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enhanced central nervous system regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent sperm axonemal central pair Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sperm axonemal central pair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal central medial nucleus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central medial nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal central pattern generator function Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal diaphragm central tendon morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal diaphragm central tendon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired central nervous system regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal central nervous system regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased central memory CD4-positive, alpha-beta T cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased central memory CD8 positive, alpha-beta T cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - PBMC - L2 - CD4+ Central Memory T Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD4+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L2 - CD8+ Central Memory T Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD8+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD4+ Central Memory T_1 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD4+ Central Memory T_2 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD4+ Central Memory T_3 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD8+ Central Memory T_1 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD8+ Central Memory T_2 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - PBMC - L3 - CD8+ Central Memory T_3 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Liver - L2 - Vascual Central Venous Endothelial Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Liver - L2 - Vascual Central Venous Endothelial cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Central memory CD4+ T cell_Arthrosis_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Arthrosis_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T helper 1 cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T helper 1 cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Peripheral blood_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell precursor_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central nervous system stem cell_Fetal brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central nervous system stem cell_Fetal brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central nervous system-associated macrophage_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central nervous system-associated macrophage_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Naïve or central memory T cell_Stomach_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Naïve or central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central nervous system cell_Central nervous system_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central nervous system cell_Central nervous system_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Heart_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Intestine_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Lymph_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lymph_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Lymphoid tissue_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Lymphoid tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Ovary_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Ovary_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Peritoneal fluid_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peritoneal fluid_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Skin_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Spleen_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Spleen_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Spleen_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Stomach_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell precursor_Stomach_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory T cell_Undefined_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD4+ T cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory CD8+ T cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Central memory regulatory T(cTreg) cell_Undefined_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Central memory regulatory T(cTreg) cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
HDAC6 interactions in the central nervous system Gene Set From WikiPathways Pathways 2024 proteins participating in the HDAC6 interactions in the central nervous system pathway from the WikiPathways Pathways 2024 dataset.
central nervous system development Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system neuron axonogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system myelination Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2025 dataset.
central tolerance induction to self antigen Gene Set From GO Biological Process Annotations 2025 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system projection neuron axonogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system neuron development Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system myelin maintenance Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system vasculogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
axonemal central apparatus assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system neuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
central nervous system myelin formation Gene Set From GO Biological Process Annotations 2025 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of central B cell tolerance induction Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
axon ensheathment in central nervous system Gene Set From GO Biological Process Annotations 2025 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of central tolerance induction Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of central B cell tolerance induction Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
Central nervous system disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autoimmune disease of central nervous system Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Central precocious puberty Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central precocious puberty from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital central hypoventilation syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital central hypoventilation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Central nervous system cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Central diabetes insipidus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central diabetes insipidus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Central nervous system disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system cancer Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune disease of central nervous system Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of central nervous system in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system vasculitis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system vasculitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune disease of central nervous system Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital central hypoventilation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital central hypoventilation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central diabetes insipidus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central diabetes insipidus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central conducting lymphatic anomaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central conducting lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central pontine myelinolysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system neuroblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system vasculitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal vein occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system hematologic cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hematologic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system tuberculosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central retinal artery occlusion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system embryonal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Solitary median maxillary central incisor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Solitary median maxillary central incisor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central corneal ulcer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system melanocytic neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system melanocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary diffuse large B-cell lymphoma of the central nervous system Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary diffuse large B-cell lymphoma of the central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system mesenchymal non-meningothelial tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central epithelioid sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central precocious puberty Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system germinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central precocious puberty 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood central nervous system embryonal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system tumor with BCOR internal tandem duplication Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central neurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central neurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system immature teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system immature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system origin vertigo Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system origin vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system mature teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system leiomyoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system lipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult central nervous system embryonal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system leiomyosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system fibrosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central precocious puberty 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system rhabdomyosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system angiosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Central nervous system Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Central nervous system Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Midbrain central gray Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Midbrain central gray in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Central amygdaloid nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Central medial thalamic nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central medial thalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Central element Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Central element cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Axonemal central apparatus Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Axonemal central apparatus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Nuclear pore central transport channel Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear pore central transport channel cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Axonemal central apparatus Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central apparatus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Axonemal central pair Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central pair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Central element Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central element cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Central vacuole Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Central cylinder Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central cylinder cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Central region of growth cone Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central region of growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Nuclear pore central transport channel Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Central hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spongy degeneration of central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongy degeneration of central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal central motor function Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal central motor function phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central precocious puberty Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Solitary median maxillary central incisor syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Solitary median maxillary central incisor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic nerve hypoplasia and abnormalities of the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central scotoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central scotoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked central congenital hypothyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked central congenital hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal dysplasia and progressive central nervous system degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central core disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central hypoventilation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypoventilation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central areolar choroidal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central areolar choroidal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrophy/Degeneration affecting the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central corneal thickness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Intraocular pressure and central corneal thickness (multi-trait analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure and central corneal thickness (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central retinal vein equivalent Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal vein equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central retinal arteriolar equivalent Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal arteriolar equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic central serous retinopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central serous retinopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric central nervous system tumors (early onset)(pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (early onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric central nervous system tumors (late onset)(pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (late onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric central nervous system tumors (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Corpus callosum central volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corpus callosum central volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Primary central nervous system lymphoma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary central nervous system lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central carbon metabolism in cancer Gene Set From KEGG Pathways 2026 proteins participating in the Central carbon metabolism in cancer pathway from the KEGG Pathways 2026 dataset.
Kallikrein, decreased urinary activity of Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallikrein, decreased urinary activity of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
decreased risk of insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased risk of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased apoptotic level Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased apoptotic level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; decreased cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; decreased cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased levels of insulin-receptor messenger ribonucleic acid Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased levels of insulin-receptor messenger ribonucleic acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased fracture risk Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased circulating c4 and predominant mesangial c4 deposition Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased circulating c4 and predominant mesangial c4 deposition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased airway responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased airway responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased chemosensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased chemosensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased glutathione production. Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased glutathione production. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased risk of cerebrovascular mortality Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased risk of cerebrovascular mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased adipocyte lipolytic function Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased adipocyte lipolytic function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased lung cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased apoptosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased apoptosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased blood pressure and plasma triglycerides Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoviral infection and decreased lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoviral infection and decreased lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased concentration of hdl-c and decreased promoter activity Gene Set From GAD Gene-Disease Associations genes associated with the disease increased concentration of hdl-c and decreased promoter activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased bone mass in patients Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased bone mass in patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased production rate of apolipoprotein a-i Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased production rate of apolipoprotein a-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term decreased in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cellular response to decreased oxygen levels Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to decreased oxygen levels biological process from the curated GO Biological Process Annotations 2015 dataset.
response to decreased oxygen levels Gene Set From GO Biological Process Annotations 2015 genes participating in the response to decreased oxygen levels biological process from the curated GO Biological Process Annotations 2015 dataset.
decreased body weight Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased fertility Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased fertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased corneal thickness Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased liver function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased liver function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased serum ceruloplasmin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased serum ceruloplasmin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased testosterone in males Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased testosterone in males phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased pulmonary function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased pulmonary function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased glucosephosphate isomerase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased glucosephosphate isomerase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased facial expression Gene Set From HPO Gene-Disease Associations genes associated with the decreased facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating aldosterone level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating aldosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating cortisol level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set From 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.
decreased adipose tissue around neck Gene Set From HPO Gene-Disease Associations genes associated with the decreased adipose tissue around neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex ii Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex iv Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex iv phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased muscle mass Gene Set From HPO Gene-Disease Associations genes associated with the decreased muscle mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fertility Gene Set From HPO Gene-Disease Associations genes associated with the decreased fertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urinary sulfate Gene Set From HPO Gene-Disease Associations genes associated with the decreased urinary sulfate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased adenosylcobalamin Gene Set From HPO Gene-Disease Associations genes associated with the decreased adenosylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased calvarial ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased calvarial ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fertility in females Gene Set From HPO Gene-Disease Associations genes associated with the decreased fertility in females phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased csf homovanillic acid (hva) Gene Set From HPO Gene-Disease Associations genes associated with the decreased csf homovanillic acid (hva) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of nadph oxidase Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of nadph oxidase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased t cell activation Gene Set From HPO Gene-Disease Associations genes associated with the decreased t cell activation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the decreased palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased numbers of nephrons Gene Set From HPO Gene-Disease Associations genes associated with the decreased numbers of nephrons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methylmalonyl-coa mutase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased methylmalonyl-coa mutase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased corneal reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased corneal reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased achilles reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased achilles reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd8+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum estradiol Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum estradiol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of small peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating acth level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating acth level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased liver function Gene Set From HPO Gene-Disease Associations genes associated with the decreased liver function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased lacrimation Gene Set From HPO Gene-Disease Associations genes associated with the decreased lacrimation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum progesterone Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum progesterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased beta-galactosidase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased beta-galactosidase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c9 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c9 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c3 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urinary urate Gene Set From HPO Gene-Disease Associations genes associated with the decreased urinary urate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of large peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased renal tubular phosphate excretion Gene Set From HPO Gene-Disease Associations genes associated with the decreased renal tubular phosphate excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of cytochrome c oxidase in muscle tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of cytochrome c oxidase in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased mitochondrial complex iii activity in liver tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased electroretinogram (erg) amplitude Gene Set From HPO Gene-Disease Associations genes associated with the decreased electroretinogram (erg) amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating renin level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating renin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum leptin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum leptin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fumarate hydratase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased fumarate hydratase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methylcobalamin Gene Set From HPO Gene-Disease Associations genes associated with the decreased methylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum ceruloplasmin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum ceruloplasmin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor b Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor b phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor h Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor h phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor i Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urine output Gene Set From HPO Gene-Disease Associations genes associated with the decreased urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased distal sensory nerve action potential Gene Set From HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased corneal thickness Gene Set From HPO Gene-Disease Associations genes associated with the decreased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased body weight Gene Set From HPO Gene-Disease Associations genes associated with the decreased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sensory nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fetal movement Gene Set From HPO Gene-Disease Associations genes associated with the decreased fetal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased testicular size Gene Set From HPO Gene-Disease Associations genes associated with the decreased testicular size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum ferritin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased cervical spine mobility Gene Set From 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.
decreased finger mobility Gene Set From HPO Gene-Disease Associations genes associated with the decreased finger mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial respiratory chain Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex iii Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex iii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd4+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd4+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased movement range in interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the decreased movement range in interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased retinal pigmentation with dispersion Gene Set From HPO Gene-Disease Associations genes associated with the decreased retinal pigmentation with dispersion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial atp synthase complex Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial atp synthase complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased purine levels Gene Set From HPO Gene-Disease Associations genes associated with the decreased purine levels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma total carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma total carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased/absent ankle reflexes Gene Set From HPO Gene-Disease Associations genes associated with the decreased/absent ankle reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased hip abduction Gene Set From HPO Gene-Disease Associations genes associated with the decreased hip abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex i Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased muscle glycogen content Gene Set From HPO Gene-Disease Associations genes associated with the decreased muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased mean platelet volume Gene Set From HPO Gene-Disease Associations genes associated with the decreased mean platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of the pyruvate dehydrogenase (pdh) complex Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of the pyruvate dehydrogenase (pdh) complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased pyruvate carboxylase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased pyruvate carboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased skull ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thymic hormone decreased Gene Set From HPO Gene-Disease Associations genes associated with the thymic hormone decreased phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased testosterone in males Gene Set From HPO Gene-Disease Associations genes associated with the decreased testosterone in males phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma free carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma free carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased patellar reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased patellar reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased cranial base ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased cranial base ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased pulmonary function Gene Set From HPO Gene-Disease Associations genes associated with the decreased pulmonary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased glomerular filtration rate Gene Set From HPO Gene-Disease Associations genes associated with the decreased glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased taste sensation Gene Set From HPO Gene-Disease Associations genes associated with the decreased taste sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased beta-glucocerebrosidase protein and activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased beta-glucocerebrosidase protein and activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased motor nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased amplitude of sensory action potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased amplitude of sensory action potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased miniature endplate potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased miniature endplate potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased subcutaneous fat Gene Set From HPO Gene-Disease Associations genes associated with the decreased subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased size of nerve terminals Gene Set From HPO Gene-Disease Associations genes associated with the decreased size of nerve terminals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sensitivity to hypoxemia Gene Set From HPO Gene-Disease Associations genes associated with the decreased sensitivity to hypoxemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased platelet glycoprotein iib-iiia Gene Set From HPO Gene-Disease Associations genes associated with the decreased platelet glycoprotein iib-iiia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methionine synthase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased methionine synthase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased adipose tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased bone mineral density of femur Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone mineral density of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased placental labyrinth size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased placental labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine urea nitrogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoclast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to viral infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating thyroid-stimulating hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythrocyte potassium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythrocyte potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating triiodothyronine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interferon-alpha level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased enteric neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased enteric neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oviduct weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oviduct weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased eosinophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone connectivity density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-17 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-17 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased compensatory feeding amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased compensatory feeding amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased percent body fat Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mean corpuscular volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mean corpuscular volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-2 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell degranulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glomerular capillary number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glomerular capillary number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of peritubular myoid cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of peritubular myoid cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryonic neuroepithelium thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryonic neuroepithelium thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igd level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igd level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased small intestinal microvillus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased striatum area Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased striatum area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trophoblast glycogen cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trophoblast glycogen cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk cell degranulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating aldosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal tubule apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal tubule apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-1 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-1 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuronal stem cell self-renewal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-12b secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-12b secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to neuronal excitotoxicity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gonadal fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ghrelin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythrocyte magnesium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythrocyte magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratinocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratinocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased blood urea nitrogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating complement protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased saturated fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased saturated fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased digestive secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased plasma cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver regeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased respiratory mucosa goblet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased systemic arterial blood pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vitamin d level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vitamin d level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced joint inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pulmonary endothelial cell surface Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary endothelial cell surface phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreas weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerular filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerular filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aggression towards mice Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aggression towards mice phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oligodendrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oligodendrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating magnesium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased a wave amplitude Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased a wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle fiber density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle fiber density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating gastrin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymph node number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ketone body level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased behavioral withdrawal response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased behavioral withdrawal response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased triiodothyronine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased length of long bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dopamine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dopamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased abdominal adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased abdominal adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating factor ix level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating factor ix level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratohyalin granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating chloride level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoid thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoid thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin turgor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin turgor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-2 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-2 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t-helper 17 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased amacrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostate gland weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased atrioventricular cushion size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased acute inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased acute inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating gonadotropin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased creatine kinase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased adrenal gland weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased adrenal gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine prostaglandin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tear production Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tear production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased axial mesoderm size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased axial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen white pulp amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatoblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatoblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondrial dna content Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondrial dna content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased chondrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased chondrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sterol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating unsaturated transferrin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating alanine transaminase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased long bone epiphyseal plate size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corticospinal tract size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bone mineral density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body mass index Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pulmonary vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased otic epithelium proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased otic epithelium proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratohyalin granule size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine major urinary protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine major urinary protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased integument system tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased integument system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased intestinal cholesterol absorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vagina weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vagina weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased extensor digitorum longus weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to kidney reperfusion injury Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tumor latency Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased epididymis weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased epididymis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-5 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-5 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased activation-induced b cell apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranium width Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranium width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostate gland duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ovulation rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ovulation rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bleeding time Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bleeding time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymphoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sensitivity to induced cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased subcutaneous adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased subcutaneous adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased incidence of tumors by chemical induction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased incidence of tumors by chemical induction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cell mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cns synapse formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fluid intake Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fluid intake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased purine-nucleoside phosphorylase activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased purine-nucleoside phosphorylase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating adrenaline level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nerve conduction velocity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nerve conduction velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tongue size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tongue size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ige level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ige level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bone fracture Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bone fracture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased serotonin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine osmolality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased otolith number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased otolith number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lipoprotein lipase activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryo size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased organ/body region tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ductal branching in the coagulating gland Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ductal branching in the coagulating gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine flow rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased double-negative t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell protease storage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell protease storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primordial ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased common myeloid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased common myeloid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryonic cilium length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryonic cilium length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine glucose level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interscapular fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic endocrine progenitor cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased luteinizing hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interferon-gamma secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interferon-gamma secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased incidence of tumors by ionizing radiation induction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased incidence of tumors by ionizing radiation induction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating atrial natriuretic factor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating atrial natriuretic factor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear nerve compound action potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear nerve compound action potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cytotoxic t cell cytolysis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cytotoxic t cell cytolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induction of seizure by inducing agent Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induction of seizure by inducing agent phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-1 beta level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased inner cell mass proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear microphonics Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear microphonics phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lean body mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased small intestinal villus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased diameter of femur Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased adrenocorticotropin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corneal stroma thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased colliculi size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased colliculi size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brain size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lumbar vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hippocampal commissure size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hippocampal commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased stereotypic behavior Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased stereotypic behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine phosphate level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic beta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic beta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cajal-retzius cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cajal-retzius cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic islet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin tensile strength Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aorta elastin content Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aorta elastin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ovary weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebellar granule cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spongiotrophoblast size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nerve fiber response threshold Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nerve fiber response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased salivation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased salivation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating creatine kinase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased energy expenditure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased energy expenditure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-6 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased survivor rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased survivor rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet calcium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased core body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased core body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating progesterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vasoconstriction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vasoconstriction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tibialis anterior weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased heart rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased heart rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to type ii hypersensitivity reaction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to type ii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased single-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased single-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating renin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thymocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thymocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased rib number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased rib number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased diameter of long bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to parasitic infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-12 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney collecting duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total retina thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased follicle stimulating hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cellular sensitivity to alkylating agents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prepulse inhibition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prepulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased paired-pulse facilitation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased paired-pulse facilitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet serotonin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostaglandin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiac output Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac output phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to experimental autoimmune myasthenia gravis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to experimental autoimmune myasthenia gravis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine aldosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-9 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-9 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung endothelial cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung endothelial cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glucagon level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sebaceous gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating creatine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiac stroke volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased clearance of atrial thrombosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased clearance of atrial thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igm level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igm level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glucocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased systemic arterial systolic blood pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating insulin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased unsaturated fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased unsaturated fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lateral semicircular canal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lateral semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased endocochlear potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased endocochlear potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythroblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interferon-gamma level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver function Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen germinal center size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen germinal center size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-4 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to experimental autoimmune uveoretinitis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine potassium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating total protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased myocardial fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased myocardial fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating bilirubin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased zigzag hair amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased zigzag hair amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebral infarction size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased threshold for auditory brainstem response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased threshold for auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-5 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased channel response intensity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased channel response intensity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased level of surface class i molecules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating prothrombin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased synaptic depression Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brown adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ceruloplasmin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ceruloplasmin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating mineralocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondria number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prolactin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tubuloglomerular feedback response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased blood uric acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased left ventricle developed pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver glycogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Harmonizome 3.0

decreased central vision Gene Set

central nervous system neoplasms; central nervous system tumors; glioma Gene Set

central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set

cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set

central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene Set

Vision Disorders Gene Set

Color Vision Defects Gene Set

Vision, Low Gene Set

binocular vision disease Gene Set

defective colour vision Gene Set

blind vision; blindness; retinal degeneration Gene Set

blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set

glaucoma, open-angle; vision disorders Gene Set

macular degeneration; vision, low Gene Set

cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set

color vision defects; retinal degeneration Gene Set

blind vision; blindness Gene Set

apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene Set

arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set

blind vision; blindness; corneal diseases; syndrome Gene Set

optic atrophy, hereditary, leber; vision disorders Gene Set

blind vision; blindness; retinal diseases Gene Set

blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set

vision Gene Set

vision Gene Set

abnormality of vision Gene Set

abnormality of binocular vision Gene Set

abnormality of vision evoked potentials Gene Set

abnormality of color vision Gene Set

blurred vision Gene Set

hemianopic blurring of vision Gene Set

Vision Gene Set

Vision Disorders Gene Set

Mesopic Vision Gene Set

Color Vision Gene Set

Color Vision Defects Gene Set

Vision, Low Gene Set

abnormal vision Gene Set

vision/eye phenotype Gene Set

The canonical retinoid cycle in rods (twilight vision) Gene Set

The retinoid cycle in cones (daylight vision) Gene Set

Abnormality Of Vision Gene Set

Low Vision Gene Set

Vision Disability Gene Set

Vision Impairment And Blindness Gene Set

Blurred Vision Gene Set

Blurred Vision, Ctcae Gene Set

Abnormal Vision Gene Set

Color Vision Defect Gene Set

Transient Unilateral Blurring Of Vision Gene Set

Abnormal Color Vision Gene Set

Color Vision Test Abnormality Gene Set

abnormal vision Gene Set

vision/eye phenotype Gene Set

The canonical retinoid cycle in rods (twilight vision) Gene Set

The retinoid cycle in cones (daylight vision) Gene Set

Binocular vision disease Gene Set

Color vision defect Gene Set

Blurred vision Gene Set

Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set

Abnormality of vision Gene Set

Computer vision syndrome Gene Set

decreased central memory CD4-positive, alpha-beta T cell number Gene Set

decreased central memory CD8 positive, alpha-beta T cell number Gene Set

central medullary reticular group, left Gene Set

precentral gyrus, right, bank of the central sulcus Gene Set

central nucleus, left Gene Set

postcentral gyrus, left, bank of the posterior central sulcus Gene Set

central nucleus, right Gene Set

central gray substance of midbrain, right Gene Set

precentral gyrus, left, bank of the central sulcus Gene Set

central gray of the pons, right Gene Set

central gray of the pons, left Gene Set

central glial substance Gene Set

postcentral gyrus, left, bank of the central sulcus Gene Set

central gray substance of midbrain, left Gene Set

central medullary reticular group, right Gene Set

postcentral gyrus, right, bank of the central sulcus Gene Set

postcentral gyrus, right, bank of the posterior central sulcus Gene Set