Large central visual field defect

Clear Filter

Results for "Large central visual field defect": 1002 gene sets

Name
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.
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.
visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Glaucomatous Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glaucomatous Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
tegmental field of p3 (Forel's field) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in tegmental field of p3 (Forel's field) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
First heart field cell(FHF)_First heart field(FHF)_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the First heart field cell(FHF)_First heart field(FHF)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Juxta-cardiac field cell_Juxta-cardiac field (JCF)_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Juxta-cardiac field cell_Juxta-cardiac field (JCF)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
visual field defects Gene Set From GAD Gene-Disease Associations genes associated with the disease visual field defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive visual field defects Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral visual field loss Gene Set From HPO Gene-Disease Associations genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Visual Field Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Field Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Visual Field Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Visual Field Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Field Test Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Field Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Field Defects Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Field Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tunnel Visual Field Constriction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tunnel Visual Field Constriction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral visual field loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral visual field loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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 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.
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.
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.
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.
drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis Gene Set From GAD Gene-Disease Associations genes associated with the disease drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set From GAD Gene-Disease Associations genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set From GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
large-cell lymphomas; lymphoma, large b-cell, diffuse Gene Set From GAD Gene-Disease Associations genes associated with the disease large-cell lymphomas; lymphoma, large b-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
CA2 field, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA2 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA1 field, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA1 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA3 field, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA3 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA4 field, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA4 field, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA3 field, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA3 field, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA2 field, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA2 field, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA4 field, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA4 field, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
CA1 field, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in CA1 field, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Field CA1, stratum radiatum Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1, stratum radiatum relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2, pyramidal layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA1, stratum lacunosum-moleculare Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1, stratum lacunosum-moleculare relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, stratum radiatum Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, stratum radiatum relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, stratum pyramidale Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, stratum pyramidale relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2, stratum oriens Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2, stratum oriens relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA1, stratum pyramidale Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1, stratum pyramidale relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, stratum oriens Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, stratum oriens relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, stratum lacunosum-moleculare Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, stratum lacunosum-moleculare relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2, stratum radiatum Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2, stratum radiatum relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2, stratum pyramidale Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2, stratum pyramidale relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA1, stratum oriens Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1, stratum oriens relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, stratum lucidum Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, stratum lucidum relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA3, pyramidal layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA3, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA2, stratum lacunosum-moleculare Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA2, stratum lacunosum-moleculare relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Field CA1, pyramidal layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Field CA1, pyramidal layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary somatosensory area, barrel field, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
field Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term field in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cardioblast migration to the midline involved in heart field formation Gene Set From GO Biological Process Annotations 2015 genes participating in the cardioblast migration to the midline involved in heart field formation biological process from the curated GO Biological Process Annotations 2015 dataset.
heart field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the heart field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
pronephric field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the pronephric field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
primary heart field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the primary heart field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
kidney field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the kidney field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
Field Dependence-Independence Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Field Dependence-Independence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
pronephric field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the pronephric field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
primary heart field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the primary heart field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
cardioblast migration to the midline involved in heart field formation Gene Set From GO Biological Process Annotations 2023 genes participating in the cardioblast migration to the midline involved in heart field formation biological process from the curated GO Biological Process Annotations 2023 dataset.
heart field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the heart field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
kidney field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the kidney field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
Posterior second heart field(pSHF) cell_Posterior second heart field_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Posterior second heart field(pSHF) cell_Posterior second heart field_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
First heart field cell_Heart_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the First heart field cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
pronephric field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the pronephric field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
primary heart field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the primary heart field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
cardioblast migration to the midline involved in heart field formation Gene Set From GO Biological Process Annotations 2025 genes participating in the cardioblast migration to the midline involved in heart field formation biological process from the curated GO Biological Process Annotations 2025 dataset.
heart field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the heart field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
kidney field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the kidney field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
Anterolateral visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Visual areas Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Visual areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posteromedial visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anteromedial visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anteromedial visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 4 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral visual area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Primary visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Posterolateral visual area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterolateral visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Anterolateral visual area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterolateral visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
IZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in primary visual cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
visual signal transduction Gene Set From Biocarta Pathways proteins participating in the visual signal transduction pathway from the Biocarta Pathways dataset.
Visual Cortex Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Visual Cortex in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual cortex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual cortex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual pathway disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease visual pathway disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
visual disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease visual disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual cortex Gene Set From GAD Gene-Disease Associations genes associated with the disease visual cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term visual in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
visual behavior Gene Set From GO Biological Process Annotations 2015 genes participating in the visual behavior biological process from the curated GO Biological Process Annotations 2015 dataset.
visual learning Gene Set From GO Biological Process Annotations 2015 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2015 dataset.
visual perception Gene Set From GO Biological Process Annotations 2015 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2015 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2015 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2015 dataset.
visual cortex disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease visual cortex disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
visual pathway disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease visual pathway disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
reduced amplitude of pattern visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal flash visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual auras Gene Set From HPO Gene-Disease Associations genes associated with the visual auras phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the absence of visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mildly reduced visual acuity Gene Set From HPO Gene-Disease Associations genes associated with the mildly reduced visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow decrease in visual acuity Gene Set From HPO Gene-Disease Associations genes associated with the slow decrease in visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual hallucinations Gene Set From HPO Gene-Disease Associations genes associated with the visual hallucinations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cortical visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the cortical visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual loss Gene Set From HPO Gene-Disease Associations genes associated with the visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged flash visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the enlarged flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
constricted visual fields Gene Set From HPO Gene-Disease Associations genes associated with the constricted visual fields phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Visual Perception Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Visual Perception phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pattern Recognition, Visual Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pattern Recognition, Visual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
the visual cycle I (vertebrates) Gene Set From HumanCyc Pathways proteins participating in the the visual cycle I (vertebrates) pathway from the HumanCyc Pathways dataset.
Visual pigments (opsins) retinal binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal visual acuity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent visual evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual pursuit Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual pursuit phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased visual acuity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal visual evoked potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Visual signal transduction: Cones Gene Set From PID Pathways proteins participating in the Visual signal transduction: Cones pathway from the PID Pathways dataset.
Visual signal transduction: Rods Gene Set From PID Pathways proteins participating in the Visual signal transduction: Rods pathway from the PID Pathways dataset.
Diseases associated with visual transduction Gene Set From Reactome Pathways 2014 proteins participating in the Diseases associated with visual transduction pathway from the Reactome Pathways dataset.
Visual phototransduction Gene Set From Reactome Pathways 2014 proteins participating in the Visual phototransduction pathway from the Reactome Pathways dataset.
visual cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue visual cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Visual Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Illusions, Visual Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Illusions, Visual in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Flash Visual Evoked Potentials Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Flash Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Pathway Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Pathway Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Auras Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Auras in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Cortex Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Cortex Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory And Visual Hallucinations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory And Visual Hallucinations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Visual Evoked Potential Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Evoked Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unspecified Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unspecified Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Timing Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Timing Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cortical Visual Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Loss Of Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Loss Of Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity, No Light Perception Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity, No Light Perception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Phenomena Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Phenomena in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Flasher - Visual Manifestation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flasher - Visual Manifestation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow Decrease In Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Decrease In Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Accommodation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Accommodation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Agnosia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Agnosia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Fixation Instability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Fixation Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Undetectable Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Undetectable Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Discomfort Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Discomfort in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mildly Reduced Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mildly Reduced Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity Light Perception With Projection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity Light Perception With Projection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonprogressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sudden Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Acuity Test Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Acuity Test Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Best Corrected Visual Acuity Test Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Best Corrected Visual Acuity Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Enlarged Flash Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Flash Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Visual Behavior For Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Visual Behavior For Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Visual Fixation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Visual Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Impairment And Blindness (Excl Colour Blindness) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment And Blindness (Excl Colour Blindness) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
visual perception Gene Set From GO Biological Process Annotations 2023 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2023 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2023 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2023 dataset.
visual learning Gene Set From GO Biological Process Annotations 2023 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2023 dataset.
visual system development Gene Set From GO Biological Process Annotations 2023 genes participating in the visual system development biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal visual evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased visual acuity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent visual evoked potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual pursuit Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual pursuit phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal visual contrast sensitivity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visual contrast sensitivity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Oligodendrocyte_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Oligodendrocyte precursor cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte precursor cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 2 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 2 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Leptomeningeal cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Leptomeningeal cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
B cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the B cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Vascular cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Vascular cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Microglial cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Microglial cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Astrocyte_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Astrocyte_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 3 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 3 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Upper layer 4 cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Upper layer 4 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
GABAergic neuron_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the GABAergic neuron_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Endothelial cell_Primary visual cortex_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Endothelial cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Defective visual phototransduction due to ABCA4 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to LRAT loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1LW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1MW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1SW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH12 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH5 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to STRA6 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset.
Diseases associated with visual transduction Gene Set From Reactome Pathways 2024 proteins participating in the Diseases associated with visual transduction pathway from the Reactome Pathways 2024 dataset.
Visual phototransduction Gene Set From Reactome Pathways 2024 proteins participating in the Visual phototransduction pathway from the Reactome Pathways 2024 dataset.
visual perception Gene Set From GO Biological Process Annotations 2025 genes participating in the visual perception biological process from the curated GO Biological Process Annotations 2025 dataset.
detection of light stimulus involved in visual perception Gene Set From GO Biological Process Annotations 2025 genes participating in the detection of light stimulus involved in visual perception biological process from the curated GO Biological Process Annotations 2025 dataset.
visual learning Gene Set From GO Biological Process Annotations 2025 genes participating in the visual learning biological process from the curated GO Biological Process Annotations 2025 dataset.
visual system development Gene Set From GO Biological Process Annotations 2025 genes participating in the visual system development biological process from the curated GO Biological Process Annotations 2025 dataset.
Visual epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual cortex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual cortex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual pathway disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual pathway disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Visual cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Visual impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral visual impairment and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral visual impairment and intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical surface area (visual PC2) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (visual PC2) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
perceptual and visual search speed (trail making test A) (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the perceptual and visual search speed (trail making test A) (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic maculopathy with decreased visual acuity in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic maculopathy with decreased visual acuity in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Dandy-Walker like malformation with atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Protan defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiac conduction defect, nonspecific Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutral 1 amino acid transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular septal defect 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular septal defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Laron-type isolated somatotropin defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neural tube defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucose-6-phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iodotyrosine deiodination defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia due to thrombomodulin defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal carnitine transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency due to defect in cd3-zeta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocyte lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iodotyrosyl coupling defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.
Cardiac Conduction Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Conduction Defect from the curated CTD Gene-Disease Associations dataset.
Atrial septal defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.
ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.
METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.
Neural tube defect, folate-sensitive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency due to Defect in CD3-Zeta Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocyte Lactate Transporter Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.
atrial heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-related birth defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital bile acid synthesis defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrial heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
qualitative platelet defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
human spermatogenic defect Gene Set From GAD Gene-Disease Associations genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
defect Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term defect in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
conotruncal defect Gene Set From GWASdb SNP-Phenotype Associations genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
thyroid hormone receptor defect Gene Set From HPO Gene-Disease Associations genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline defect of mandible Gene Set From HPO Gene-Disease Associations genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vertebral segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set From HPO Gene-Disease Associations genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
secundum atrial septal defect Gene Set From HPO Gene-Disease Associations genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dynein arm defect of respiratory motile cilia Gene Set From HPO Gene-Disease Associations genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inlet ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thyroid defect in oxidation and organification of iodide Gene Set From HPO Gene-Disease Associations genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenocorticotropin (acth) receptor (acthr) defect Gene Set From HPO Gene-Disease Associations genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sacral segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abdominal wall defect Gene Set From HPO Gene-Disease Associations genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
defect in the atrial septum Gene Set From HPO Gene-Disease Associations genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital septal defect Gene Set From HPO Gene-Disease Associations genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skull defect Gene Set From HPO Gene-Disease Associations genes associated with the skull defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypotonia due to defect at the neuromuscular junction Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cervical segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
perimembranous ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline defect of the nose Gene Set From HPO Gene-Disease Associations genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
conotruncal defect Gene Set From HPO Gene-Disease Associations genes associated with the conotruncal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
primum atrial septal defect Gene Set From HPO Gene-Disease Associations genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mannose-P-dolichol utilization defect 1 protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
perimembraneous ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inlet ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iodide oxidation defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aorticopulmonary septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle, ventricular defect committed to aorta Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ostium primum atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ostium secundum atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thrombophilia due to thrombomodulin defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder due to p2rx1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
schizophrenia, neurophysiologic defect in Gene Set From OMIM Gene-Disease Associations genes associated with the schizophrenia, neurophysiologic defect in phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrioventricular septal defect, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
?isolated growth hormone deficiency due to defect in ghrf Gene Set From OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocyte lactate transporter defect Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset.
natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set From OMIM Gene-Disease Associations genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
selective t-cell defect Gene Set From OMIM Gene-Disease Associations genes associated with the selective t-cell defect phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 6 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 5 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 2 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 1 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 9 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 8 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiac conduction defect, nonspecific Gene Set From OMIM Gene-Disease Associations genes associated with the cardiac conduction defect, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.
rickets due to defect in vitamin d 25-hydroxylation Gene Set From OMIM Gene-Disease Associations genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrioventricular septal defect, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
oocyte maturation defect Gene Set From OMIM Gene-Disease Associations genes associated with the oocyte maturation defect phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria due to transcobalamin receptor defect Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 5 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia, x-linked, due to factor ix defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 7, with or without av conduction defects Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency due to defect in mapbp-interacting protein Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, familial, due to ttf-1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to thrombin defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.
{cardiac conduction defect, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {cardiac conduction defect, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.
Histidinuria Renal Tubular Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histidinuria Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Acid Synthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Carnitine Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Carnitine Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortopulmonary Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortopulmonary Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrial Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ostium Secundum Atrial Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ostium Secundum Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol Related Birth Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucose-6-Phosphate Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucose-6-Phosphate Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ventilatory Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Calvarial Skull Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Single Ventricle Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Single Ventricle Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Defect Of Skull And Scalp Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of Skull And Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Sinus Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Sinus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Ventricular Septum Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perimembranous Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perimembranous Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triple Gene Defect Alpha Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triple Gene Defect Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defect Of Vertebral Segmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Vertebral Segmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycosylphosphatidylinositol Biosynthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycosylphosphatidylinositol Biosynthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Or Persistent Ostium Secundum Defect (Type Ii) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Ostium Secundum Defect (Type Ii) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Or Persistent Sinus Venosus Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Sinus Venosus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antibody Deficiency Due To Defect In Cd19 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Conotruncal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Conotruncal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Ventilatory Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Defect Of Atrioventricular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Defect Of Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synthetic Defect Of Bile Acids Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Synthetic Defect Of Bile Acids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Bile Acid Synthesis Defect Type 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Bile Acid Synthesis Defect Type 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transitional Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transitional Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Bundle Branch System Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Bundle Branch System Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midline Defect Of The Nose Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midline Defect Of The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Plasma Membrane Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Plasma Membrane Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defect Of Articular Cartilage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Articular Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoracoabdominal Wall Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Wall Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Atresia With Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Atresia With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Membranous Ventricular Septum Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Membranous Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Defect Of The Pericardium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of The Pericardium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insulin Receptor, Defect In Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insulin Receptor, Defect In in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iodide Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iodide Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neural Tube Defect, Folate-Sensitive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neural Tube Defect, Folate-Sensitive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adenosylcobalamin Synthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adenosylcobalamin Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oocyte Maturation Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oocyte Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sacral Defect And Anterior Sacral Meningocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sacral Defect And Anterior Sacral Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Tubular Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Valvular Defect, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ulnar-Fibular Ray Defect And Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ulnar-Fibular Ray Defect And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Defect, Nonprogressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect, Nonprogressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrinolytic Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrinolytic Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erythrocyte Lactate Transporter Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythrocyte Lactate Transporter Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mondini Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mondini Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart Defect, Tongue Hamartoma And Polysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defect, Tongue Hamartoma And Polysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mucociliary Clearance Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mucociliary Clearance Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenocorticotropin Receptor Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adrenocorticotropin Receptor Defect 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.
Maturation Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Restrictive Ventilatory Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restrictive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Heart Defect (In Some Patients) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heart Defect (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cardiac Conduction Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dynein Arm Defect Of Respiratory Motile Cilia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dynein Arm Defect Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iris Transillumination Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iris Transillumination Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iodide Organification Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iodide Organification Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Segmentation Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Segmentation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lacrimal Duct Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Duct Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unbalanced Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unbalanced Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Afferent Pupillary Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Afferent Pupillary Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventral Septal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventral Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thyroid Defect In Oxidation And Organification Of Iodide Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thyroid Defect In Oxidation And Organification Of Iodide in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Activating Thyroid-Stimulating Hormone Receptor Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Activating Thyroid-Stimulating Hormone Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
perimembraneous ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ostium secundum atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscular ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ostium primum atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
inlet ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aorticopulmonary septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
iodide oxidation defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
partial atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle, ventricular defect committed to aorta Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle, noncommitted ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, noncommitted ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subarterial ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subarterial ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
repair of mitotic kinetochore microtubule attachment defect Gene Set From GO Biological Process Annotations 2025 genes participating in the repair of mitotic kinetochore microtubule attachment defect biological process from the curated GO Biological Process Annotations 2025 dataset.
Atrial heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Atrial heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neural tube defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neural tube defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neural tube defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neural tube defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycosylphosphatidylinositol biosynthesis defect 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycosylphosphatidylinositol biosynthesis defect 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Qualitative platelet defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Joubert syndrome with orofaciodigital defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Joubert syndrome with orofaciodigital defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked thrombophilia due to factor IX defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental cardiac valvular defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotrichosis-lymphedema-telangiectasia-renal defect syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombomodulin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nerve fibre bundle defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nerve fibre bundle defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroglobulin synthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroglobulin synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iodotyrosine deiodination defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neutral 1 amino acid transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital bile acid synthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bile acid synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iris transillumination defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iris transillumination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrial septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrial septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal carnitine transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glucose-6-phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peroxisome biogenesis disorder due to PEX1 defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Laron- somatotropin defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Laron- somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations 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.
Protan defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iodotyrosyl coupling defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MPV17-related mitochondrial DNA maintenance defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MPV17-related mitochondrial DNA maintenance defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neural tube defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gastrointestinal defect and immunodeficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastrointestinal defect and immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Single Ventricle Defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Single Ventricle Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Heart defect - tongue hamartoma - polysyndactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Heart defect - tongue hamartoma - polysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy due to lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic acidemia due to transcobalamin receptor defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sacral defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sacral defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bile acid conjugation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile acid conjugation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ulnar/fibula ray defect-brachydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ulnar/fibula ray defect-brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to defect in CD3-gamma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to defect in CD3-gamma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroid Hormonogenesis Defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroid Hormonogenesis Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycosylphosphatidylinositol biosynthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycosylphosphatidylinositol biosynthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular septal defect and common atrioventricular junction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiac valvular defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac valvular defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile arthritis due to defect in LA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile arthritis due to defect in LA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Female infertility due to zona pellucida defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (inherited effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
central medullary reticular group, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
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.
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.
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 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.
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.
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.
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.
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.

Harmonizome 3.0

large central visual field defect Gene Set

Large Central Visual Field Defect Gene Set

visual field defect Gene Set

Glaucomatous Visual Field Defect Gene Set

tegmental field of p3 (Forel's field) Gene Set

First heart field cell(FHF)_First heart field(FHF)_Mouse Gene Set

Juxta-cardiac field cell_Juxta-cardiac field (JCF)_Mouse Gene Set

visual field defects Gene Set

progressive visual field defects Gene Set

peripheral visual field loss Gene Set

Visual Field Constriction Gene Set

Peripheral Visual Field Loss Gene Set

Abnormal Visual Field Test Gene Set

Progressive Visual Field Defects Gene Set

Tunnel Visual Field Constriction Gene Set

Peripheral visual field loss Gene Set

sudden central visual loss Gene Set

progressive central visual loss Gene Set

Central Visual Impairment 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

Diffuse Large B-Cell Lymphoma Of Central Nervous System Gene Set

Primary diffuse large B-cell lymphoma of the central nervous system Gene Set

drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis Gene Set

b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous Gene Set

large-cell lymphomas; lymphoma, large b-cell, diffuse Gene Set

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; translocation, genetic Gene Set

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse Gene Set

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

CA2 field, right Gene Set

CA1 field, right Gene Set

CA3 field, right Gene Set

CA4 field, right Gene Set

CA3 field, left Gene Set

CA2 field, left Gene Set

CA4 field, left Gene Set

CA1 field, left Gene Set

Field CA1, stratum radiatum Gene Set

Field CA2, pyramidal layer Gene Set

Field CA1, stratum lacunosum-moleculare Gene Set

Field CA3, stratum radiatum Gene Set

Field CA3, stratum pyramidale Gene Set

Field CA2, stratum oriens Gene Set

Primary somatosensory area, barrel field, layer 2/3 Gene Set

Field CA1, stratum pyramidale Gene Set

Field CA3, stratum oriens Gene Set

Field CA3, stratum lacunosum-moleculare Gene Set

Field CA1 Gene Set

Field CA3 Gene Set

Field CA2 Gene Set

Field CA2, stratum radiatum Gene Set

Field CA2, stratum pyramidale Gene Set

Primary somatosensory area, barrel field Gene Set

Field CA1, stratum oriens Gene Set

Field CA3, stratum lucidum Gene Set

Field CA3, pyramidal layer Gene Set

Primary somatosensory area, barrel field, layer 6b Gene Set

Primary somatosensory area, barrel field, layer 6a Gene Set

Field CA2, stratum lacunosum-moleculare Gene Set

Field CA1, pyramidal layer Gene Set

Primary somatosensory area, barrel field, layer 1 Gene Set

Primary somatosensory area, barrel field, layer 5 Gene Set

Primary somatosensory area, barrel field, layer 4 Gene Set

field Gene Set

cardioblast migration to the midline involved in heart field formation Gene Set

heart field specification Gene Set

pronephric field specification Gene Set

primary heart field specification Gene Set

regulation of secondary heart field cardioblast proliferation Gene Set

notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation Gene Set

kidney field specification Gene Set

positive regulation of secondary heart field cardioblast proliferation Gene Set

secondary heart field specification Gene Set

Field Dependence-Independence Gene Set