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abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Central Somatosensory Evoked Potentials Gene SetFrom 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. |
abnormality of somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Somatosensory Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Giant Somatosensory Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Giant Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prolonged Somatosensory Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormality of vision evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced amplitude of pattern visual evoked potentials Gene SetFrom 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 SetFrom 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. |
absence of visual evoked potentials Gene SetFrom 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. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
prolonged brainstem auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the prolonged brainstem auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged flash visual evoked potentials Gene SetFrom 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. |
Abnormal Flash Visual Evoked Potentials Gene SetFrom 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. |
Abnormal Timing Of Pattern Reversal Visual Evoked Potentials Gene SetFrom 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. |
Undetectable Visual Evoked Potentials Gene SetFrom 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. |
Abnormal Lower-Limb Motor Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lower-Limb Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Motor Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Motor Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials Gene SetFrom 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. |
Enlarged Flash Visual Evoked Potentials Gene SetFrom 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. |
Prolonged Brainstem Auditory Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Brainstem Auditory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
central nervous system neoplasms; central nervous system tumors; glioma Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
p300 potentials Gene SetFrom GAD Gene-Disease Associations genes associated with the disease p300 potentials in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
potentials Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term potentials in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
decreased amplitude of sensory action potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased amplitude of sensory action potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased miniature endplate potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased miniature endplate potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired ability to fire action potentials Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Decreased Miniature Endplate Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Miniature Endplate Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Amplitude Of Sensory Action Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Amplitude Of Sensory Action Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
impaired ability to fire action potentials Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
auditory evoked potential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease auditory evoked potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
evoked Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term evoked in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
gaze-evoked horizontal nystagmus Gene SetFrom HPO Gene-Disease Associations genes associated with the gaze-evoked horizontal nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gaze-evoked nystagmus Gene SetFrom HPO Gene-Disease Associations genes associated with the gaze-evoked nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent visual evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent linear vestibular evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced linear vestibular evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal linear vestibular evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual evoked potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Visual Evoked Potential Gene SetFrom 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. |
Gaze-Evoked Horizontal Nystagmus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gaze-Evoked Horizontal Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Auditory Evoked Potential Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Auditory Evoked Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
reduced linear vestibular evoked potential Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal visual evoked potential Gene SetFrom 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. |
absent linear vestibular evoked potential Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal linear vestibular evoked potential Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal linear vestibular evoked potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent visual evoked potential Gene SetFrom 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. |
evoked excitatory postsynaptic potential Gene SetFrom GO Biological Process Annotations 2025 genes participating in the evoked excitatory postsynaptic potential biological process from the curated GO Biological Process Annotations 2025 dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom 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. |
abnormality of central motor function Gene SetFrom 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. |
Abnormality Of Central Sensory Function Gene SetFrom 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 SetFrom 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. |
Primary somatosensory area, trunk Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Supplemental somatosensory area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Supplemental somatosensory area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Somatosensory areas Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Somatosensory areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area 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 SetFrom 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. |
Primary somatosensory area, upper limb Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Supplemental somatosensory area, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Supplemental somatosensory area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field Gene SetFrom 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. |
Primary somatosensory area, lower limb, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, 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 6b Gene SetFrom 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 SetFrom 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. |
Primary somatosensory area, trunk, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, 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 1 Gene SetFrom 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 SetFrom 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 SetFrom 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. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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. |
primary somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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 somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_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. |
SP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Somatosensory Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Somatosensory Disorders from the curated CTD Gene-Disease Associations dataset. |
hiv infections; neuritis; somatosensory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; neuritis; somatosensory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
somatosensory Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term somatosensory in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
absent barrels in primary somatosensory cortex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent barrels in primary somatosensory cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatosensory cortex morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatosensory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary somatosensory cortex morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary somatosensory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
somatosensory cortex Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue somatosensory cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Seizures, Somatosensory Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Somatosensory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal somatosensory cortex morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatosensory cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent barrels in primary somatosensory cortex Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent barrels in primary somatosensory cortex phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatosensory cortex physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatosensory cortex physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal primary somatosensory cortex morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal primary somatosensory cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Somatosensory cortex Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Somatosensory cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
central medullary reticular group, left Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital central hypoventilation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central precocious puberty Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central core disease Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
central element Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom 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 SetFrom 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. |
atrophy/degeneration affecting the central nervous system Gene SetFrom 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 SetFrom 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 SetFrom 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. |
malignant neoplasm of the central nervous system Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
central hypothyroidism Gene SetFrom 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 SetFrom 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 SetFrom 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. |
lipomas of the central neryous system Gene SetFrom 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. |
sudden central visual loss Gene SetFrom 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 SetFrom HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central apnea Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large central visual field defect Gene SetFrom HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Central Serous Chorioretinopathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Visual Impairment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Central Serous Chorioretinopathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Auditory Processing Disorder, Central in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Large B-Cell Lymphoma Of Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Apnea Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Central Vertebral Hypoplasia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Cyanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Central Visual Field Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Core Regions In Muscle Fibers Gene SetFrom 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. |
Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Affecting The Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
central nervous system development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelination Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2023 dataset. |
central tolerance induction to self antigen Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system projection neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system vasculogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
axonemal central apparatus assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
axon ensheathment in central nervous system Gene SetFrom GO Biological Process Annotations 2023 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal spinal cord central canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sperm axonemal central pair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sperm axonemal central pair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central medial nucleus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central medial nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central pattern generator function Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal diaphragm central tendon morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal diaphragm central tendon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased central memory CD4-positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased central memory CD8 positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased central memory CD4-positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased central memory CD8 positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - PBMC - L2 - CD4+ Central Memory T Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD4+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L2 - CD8+ Central Memory T Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD8+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Liver - L2 - Vascual Central Venous Endothelial Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Liver - L2 - Vascual Central Venous Endothelial cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Central memory CD4+ T cell_Arthrosis_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Arthrosis_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T helper 1 cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T helper 1 cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peripheral blood_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell precursor_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system stem cell_Fetal brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system stem cell_Fetal brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system-associated macrophage_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system-associated macrophage_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Naïve or central memory T cell_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Naïve or central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system cell_Central nervous system_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system cell_Central nervous system_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Heart_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Intestine_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lymph_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lymph_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Lymphoid tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Lymphoid tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Ovary_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Ovary_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peritoneal fluid_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peritoneal fluid_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Spleen_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Spleen_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Spleen_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell precursor_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory regulatory T(cTreg) cell_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory regulatory T(cTreg) cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
HDAC6 interactions in the central nervous system Gene SetFrom WikiPathways Pathways 2024 proteins participating in the HDAC6 interactions in the central nervous system pathway from the WikiPathways Pathways 2024 dataset. |
central nervous system development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelination Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2025 dataset. |
central tolerance induction to self antigen Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system projection neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system vasculogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
axonemal central apparatus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
axon ensheathment in central nervous system Gene SetFrom GO Biological Process Annotations 2025 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central precocious puberty Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central precocious puberty from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital central hypoventilation syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital central hypoventilation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central diabetes insipidus Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central diabetes insipidus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of central nervous system in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system vasculitis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system vasculitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital central hypoventilation syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital central hypoventilation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central diabetes insipidus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central diabetes insipidus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central conducting lymphatic anomaly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central conducting lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central pontine myelinolysis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system neuroblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system vasculitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central retinal vein occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central sleep apnea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system hematologic cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hematologic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central retinal artery occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial central choroid dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Solitary median maxillary central incisor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Solitary median maxillary central incisor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system melanocytic neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system melanocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary diffuse large B-cell lymphoma of the central nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary diffuse large B-cell lymphoma of the central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system mesenchymal non-meningothelial tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central epithelioid sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system germinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system tumor with BCOR internal tandem duplication Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central neurocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central neurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system immature teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system immature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system origin vertigo Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system origin vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system mature teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adult central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system fibrosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system rhabdomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system angiosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Midbrain central gray Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Midbrain central gray in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central amygdaloid nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central medial thalamic nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central medial thalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central element Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Central element cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Axonemal central apparatus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Axonemal central apparatus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore central transport channel Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear pore central transport channel cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Axonemal central apparatus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central apparatus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Axonemal central pair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central pair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central element Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central element cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central vacuole Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central cylinder Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central cylinder cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central region of growth cone Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central region of growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore central transport channel Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central hypotonia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spongy degeneration of central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongy degeneration of central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal central motor function Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal central motor function phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central precocious puberty Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital central hypoventilation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Solitary median maxillary central incisor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Solitary median maxillary central incisor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Optic nerve hypoplasia and abnormalities of the central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central scotoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central scotoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked central congenital hypothyroidism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked central congenital hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skeletal dysplasia and progressive central nervous system degeneration Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central core disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central hypoventilation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypoventilation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central areolar choroidal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central areolar choroidal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atrophy/Degeneration affecting the central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central corneal thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure and central corneal thickness (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure and central corneal thickness (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central retinal vein equivalent Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal vein equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central retinal arteriolar equivalent Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal arteriolar equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic central serous retinopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central serous retinopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (early onset)(pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (early onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (late onset)(pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (late onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corpus callosum central volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corpus callosum central volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Primary central nervous system lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary central nervous system lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central carbon metabolism in cancer Gene SetFrom KEGG Pathways 2026 proteins participating in the Central carbon metabolism in cancer pathway from the KEGG Pathways 2026 dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |