| Name |
|---|
FCMTE2 Genefamilial cortical myoclonic tremor with epilepsy 2 |
FCMTE1 Genefamilial cortical myoclonic tremor with epilepsy 1 |
ETL6 GeneEpilepsy, familial temporal lobe, 6 |
ETL2 Geneepilepsy, familial temporal lobe |
FMTLE GeneEpilepsy, familial mesial temporal lobe |
temporal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Temporal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Occipital cortical area (total cortical area interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Occipital cortical area (total cortical area interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
posterior cortical atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebellar cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Cerebral Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Cortical Atrophy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Late Cortical Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Parietal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral cortical atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Posterior cortical atrophy and Alzheimer's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior cortical atrophy and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
temporal lobe atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
muscular atrophy, spinal; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical subplate Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical subplate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of PrS (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of PrS (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of OCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of OCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of InsCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of InsCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of PCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of PCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of PaS (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of PaS (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
dorsal cortical nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal cortical nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal cortical nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in internal cortical nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posteromedial cortical amygdaloid area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posteromedial cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
external cortical nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in external cortical nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, anterior part, layer 2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical plate Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, anterior part, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterolateral cortical amygdaloid area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterolateral cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of CCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of CCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, anterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of ERCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of ERCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
superficial stratum of FCx (cortical plate/marginal zone) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of FCx (cortical plate/marginal zone) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
anterior cortical amygdaloid area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
anterior cortical nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
posterior cortical nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Myoclonus, familial cortical Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical malformations, occipital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical malformations, occipital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia-focal epilepsy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile cortical hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
cortical granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cortical granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical endoplasmic reticulum Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cortical endoplasmic reticulum cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical actin cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cortical actin cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cortical cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical microtubule cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cortical microtubule cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
medial cortical node Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the medial cortical node cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical endoplasmic reticulum Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical endoplasmic reticulum cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical lewy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical microtubule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical microtubule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical actin cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical actin cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
actin cortical patch Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the actin cortical patch cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical microtubule cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical microtubule cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Kir4.1-beta-dystroglycan complex, cortical astrocytes Gene Setproteins in the Kir4.1-beta-dystroglycan complex, cortical astrocytes protein complex from the CORUM Protein Complexes dataset. |
Kir4.1-alpha-1-syntrophin complex, cortical astrocytes Gene Setproteins in the Kir4.1-alpha-1-syntrophin complex, cortical astrocytes protein complex from the CORUM Protein Complexes dataset. |
Kir4.1-dystrophin complex, cortical astrocytes Gene Setproteins in the Kir4.1-dystrophin complex, cortical astrocytes protein complex from the CORUM Protein Complexes dataset. |
Focal cortical dysplasia of Taylor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Focal cortical dysplasia of Taylor from the curated CTD Gene-Disease Associations dataset. |
Blindness, Cortical Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blindness, Cortical from the curated CTD Gene-Disease Associations dataset. |
Cortical Dysplasia-Focal Epilepsy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Cataract, Age-Related Cortical, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset. |
Cataract, Cortical, Juvenile-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset. |
Malformations of Cortical Development Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malformations of Cortical Development from the curated CTD Gene-Disease Associations dataset. |
Hyperostosis, Cortical, Congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperostosis, Cortical, Congenital from the curated CTD Gene-Disease Associations dataset. |
cortical blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cortical blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cortical thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cortical thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adrenal cortical hypofunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adrenal cortical hypofunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adrenal cortical adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adrenal cortical adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cortical deafness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cortical deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
predominantly cortical thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease predominantly cortical thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malformations of cortical development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malformations of cortical development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cortical surface area Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cortical surface area in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
verbal learning, verbal memory, and regional cortical gray matter density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal cortex neoplasms; adrenal cortical adenoma; adrenocortical adenoma; hyperaldosteronism; tumors of adrenal cortex Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal cortex neoplasms; adrenal cortical adenoma; adrenocortical adenoma; hyperaldosteronism; tumors of adrenal cortex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cortical Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term cortical in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
MECP2_KD_GDS4759_334_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MECP2_KD_GDS4759_334_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
FMR1_KD_GDS4759_333_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the FMR1_KD_GDS4759_333_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
MEF2A_KD_GDS4759_340_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MEF2A_KD_GDS4759_340_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
NLGN3_KD_GDS4759_336_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NLGN3_KD_GDS4759_336_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
MEF2D_KD_GDS4759_339_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MEF2D_KD_GDS4759_339_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
SHANK3_KD_GDS4759_338_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SHANK3_KD_GDS4759_338_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
NLGN1_KD_GDS4759_335_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NLGN1_KD_GDS4759_335_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PTEN_KD_GDS4759_337_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_KD_GDS4759_337_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical actin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cortical actin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical microtubule organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cortical microtubule organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cortical cytoskeleton organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cortical collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical granule Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cortical granule cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cortical endoplasmic reticulum Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cortical endoplasmic reticulum cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cortical cytoskeleton Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cortical cytoskeleton cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cortical actin cytoskeleton Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cortical actin cytoskeleton cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cortical microtubule cytoskeleton Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cortical microtubule cytoskeleton cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Cortical thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Cortical thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Entorhinal cortical thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Entorhinal cortical thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Cortical structure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Cortical structure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
cortical sclerosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the cortical sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
cortical tubers Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical tubers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical gyral simplification Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical gyral simplification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical thickening of long bone diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical thickening of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical irregularity Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontoparietal cortical dysplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical dysplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral cortical neurodegeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral cortical neurodegeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
juvenile cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the juvenile cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dense posterior cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the dense posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diaphyseal cortical sclerosis Gene SetFrom HPO Gene-Disease Associations genes associated with the diaphyseal cortical sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical visual impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical pulverulent cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical microcysts Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical microcysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical adenoma Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical adenoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Malformations of Cortical Development Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Malformations of Cortical Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal cortical plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cortical intermediate zone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical intermediate zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized cortical plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized cortical plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cortical renal glomerulopathies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cortical renal glomerulopathies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased adrenal cortical tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased adrenal cortical tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cortical ventricular zone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical ventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin cortical plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin cortical plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
adrenal cortical hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the adrenal cortical hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cortical marginal zone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical marginal zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
anterior cortical cataracts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the anterior cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cortical cataracts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
focal cortical dysplasia, taylor balloon cell type Gene SetFrom OMIM Gene-Disease Associations genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset. |
{cataract 28, age-related cortical, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {cataract 28, age-related cortical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia-focal epilepsy syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia-focal epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical malformations, occipital Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical malformations, occipital phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myoclonus, familial cortical Gene SetFrom OMIM Gene-Disease Associations genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset. |
adrenal cortical carcinoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the adrenal cortical carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cortical in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
thymic cortical epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thymic cortical epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cerebral cortical neuron Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebral cortical neuron in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cortical collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cortical collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cortical collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cortical collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cortical amygdaloid nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cortical amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Cortical Congenital Hyperostosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Congenital Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adrenal Cortical Hypofunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adrenal Cortical Hypofunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adrenal Cortical Adenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adrenal Cortical Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malformations Of Cortical Development Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malformations Of Cortical Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Cortical Hemiatrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Hemiatrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Cortical Bone Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Cortical Bone Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Focal Cortical Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Diaphyseal Thickening Of The Upper Limbs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Diaphyseal Thickening Of The Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Age-Related Cortical Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical, Lamellar, Or Zonular Nonsenile Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical, Lamellar, Or Zonular Nonsenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Cortical Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Adenoma Of Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Adenoma Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Dysplasia With Focal Epilepsy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Dysplasia With Focal Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Hyperostosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Irregularity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Irregularity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Thickening Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Thickening Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Displasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Displasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Focal Cortical Dysplasia Type Iia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Type Iia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Focal Cortical Dysplasia Type Iib Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Type Iib in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Malformations, Occipital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Malformations, Occipital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Pulverulent Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Pulverulent Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Focal Cortical Dysplasia Of Taylor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Focal Cortical Dysplasia Of Taylor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Isolated Focal Cortical Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Isolated Focal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontoparietal Cortical Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontoparietal Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Cortical Gyration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Cortical Gyration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Visual Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Gyral Simplification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Gyral Simplification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diaphyseal Cortical Sclerosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diaphyseal Cortical Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Malformations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Renal Cortical Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Cortical Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Sclerosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Subperiosteal Resorption Of Humeral Metaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Subperiosteal Resorption Of Humeral Metaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortical Tubers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Tubers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Renal Cortical Microcysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Cortical Microcysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dense Posterior Cortical Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dense Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Cortical Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Cortical Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cerebral Cortical Neurodegeneration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebral Cortical Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Humeral Cortical Thickening Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Humeral Cortical Thickening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
cortical actin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cortical actin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
cortical microtubule organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cortical microtubule organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
cortical cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cortical cytoskeleton organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
cortical actin cytoskeleton Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical actin cytoskeleton cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cortical endoplasmic reticulum Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical endoplasmic reticulum cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cortical cytoskeleton Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical cytoskeleton cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cortical granule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical granule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cortical microtubule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical microtubule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cortical microtubule cytoskeleton Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cortical microtubule cytoskeleton cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
CDKN2AIP-20523734-CORTICAL-NEURONS Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the CDKN2AIP-20523734-CORTICAL-NEURONS transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
abnormal cortical marginal zone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cortical marginal zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin cortical plate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cortical plate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cortical plate morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cortical plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cortical renal glomerulopathies Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cortical renal glomerulopathies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cortical cataract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cortical ventricular zone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cortical ventricular zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
adrenal cortical hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the adrenal cortical hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized cortical plate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized cortical plate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
anterior cortical cataract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cortical intermediate zone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cortical intermediate zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
posterior cortical cataract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ectopic cortical neuron Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic cortical neuron phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased adrenal cortical tumor incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased adrenal cortical tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L2 - Cortical Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Cortical Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Cortical Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Cortical Vascular Smooth Muscle / Pericyte Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Vascular Smooth Muscle / Pericyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Vascular Smooth Muscle / Pericyte Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Vascular Smooth Muscle / Pericyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Cortical cell_Cortex_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical cell_Cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical somatostatin (SST) interneuron_Brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical somatostatin (SST) interneuron_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer cortical neuron_Cortex_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer cortical neuron_Cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical stromal cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical stromal cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Interstitial Cell (Cortical)_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Interstitial Cell (Cortical)_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical thick ascending limb cell (CTAL cell)_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical thick ascending limb cell (CTAL cell)_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical thymus epithelial cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical thymus epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical thymic epithelial cell_Thymus_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical thymic epithelial cell_Thymus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Immature cortical thymic epithelial cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Immature cortical thymic epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Cortical neuron_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Cortical neuron_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Regulation of cortical dendrite branching Gene Setproteins participating in the Regulation of cortical dendrite branching pathway from the Reactome Pathways 2024 dataset. |
cortical actin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cortical actin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
cortical microtubule organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cortical microtubule organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
cortical granule exocytosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cortical granule exocytosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
cortical cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cortical cytoskeleton organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
cortical actin cytoskeleton Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical actin cytoskeleton cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical endoplasmic reticulum Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical endoplasmic reticulum cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical microtubule plus-end Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical microtubule plus-end cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical cytoskeleton Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical cytoskeleton cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical granule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical granule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical microtubule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical microtubule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cortical microtubule cytoskeleton Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cortical microtubule cytoskeleton cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Adrenal cortical hypofunction Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Adrenal cortical hypofunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Adrenal cortical hypofunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adrenal cortical hypofunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adrenal cortical adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adrenal cortical adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cortical blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Predominantly cortical thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Predominantly cortical thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary autosomal recessive microcephaly 2 with or without cortical malformations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary autosomal recessive microcephaly 2 with or without cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cortical deafness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adrenal cortical adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adrenal cortical adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cortical dysplasia-focal epilepsy syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical dysplasia-focal epilepsy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cortical senile cataract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cerebral cortical neuron Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebral cortical neuron in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cortical collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cortical collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Thymic cortical epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thymic cortical epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical amygdaloid nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cortical amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical endoplasmic reticulum Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical endoplasmic reticulum cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical actin cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical actin cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule plus-end Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical microtubule plus-end cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical microtubule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical microtubule cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cortical granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cortical granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical microtubule cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical actin cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical actin cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical Lewy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical Lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical endoplasmic reticulum Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical endoplasmic reticulum cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Medial cortical node Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Medial cortical node cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cdr2 medial cortical node complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cdr2 medial cortical node complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Actin cortical patch Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Actin cortical patch cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical microtubule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cortical microtubule plus-end Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cortical microtubule plus-end cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Lateral cortical node Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lateral cortical node cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Isolated focal cortical dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated focal cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical dysplasia-focal epilepsy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Complex cortical dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Complex cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile cortical hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical tubers Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical tubers phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal cortical cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cortical cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal cortical gyration Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cortical gyration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Focal cortical dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Age-related cortical cataract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Age-related cortical cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical pulverulent cataract Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical pulverulent cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical thickness (MOSTest) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical thickness (MOSTest) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical surface area (min-P) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (min-P) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical thickness (min-P) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical thickness (min-P) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical surface area (MOSTest) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (MOSTest) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cingulate cortical amyloid beta load Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cingulate cortical amyloid beta load phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Entorhinal cortical thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Entorhinal cortical thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Entorhinal cortical volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Entorhinal cortical volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Entorhinal cortical thickness (Alzheimer's disease interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Entorhinal cortical thickness (Alzheimer's disease interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Entorhinal cortical volume (Alzheimer's disease interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Entorhinal cortical volume (Alzheimer's disease interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical surface area (visual PC2) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (visual PC2) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical surface area (global PC1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (global PC1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cerebral cortical growth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebral cortical growth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Right lateral prefrontal cortical growth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Right lateral prefrontal cortical growth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical surface area Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sub-cortical grey matter volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sub-cortical grey matter volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cortical amyloid beta load Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical amyloid beta load phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
temporal pole, right, inferior aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, right, inferior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, right, bank of mts Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, right, bank of mts relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, right, bank of the its Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, right, bank of the its relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
temporal pole, left, superior aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, left, superior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
superior temporal gyrus, left, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior temporal gyrus, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
temporal pole, left, medial aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, left, medial aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, left, bank of mts Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, left, bank of mts relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
middle temporal gyrus, right, superior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in middle temporal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
middle temporal gyrus, right, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in middle temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
occipito-temporal gyrus, left, superior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipito-temporal gyrus, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
superior temporal gyrus, right, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
superior temporal gyrus, right, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior temporal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
middle temporal gyrus, left, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in middle temporal gyrus, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
occipito-temporal gyrus, left, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipito-temporal gyrus, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
occipito-temporal gyrus, right, inferior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipito-temporal gyrus, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
occipito-temporal gyrus, right, superior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in occipito-temporal gyrus, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, left, bank of the its Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, left, bank of the its relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, right, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
temporal pole, right, medial aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, right, medial aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
superior temporal gyrus, left, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in superior temporal gyrus, left, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
inferior temporal gyrus, left, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in inferior temporal gyrus, left, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
middle temporal gyrus, left, superior bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in middle temporal gyrus, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
temporal pole, right, superior aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, right, superior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
temporal pole, left, inferior aspect Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in temporal pole, left, inferior aspect relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
Temporal association areas Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Temporal association areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
temporal muscle trigeminal motor cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in temporal muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Temporal association areas, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Temporal association areas, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Temporal association areas, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Temporal association areas, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
temporal neocortex_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in temporal neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
temporal neocortex_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in temporal neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_4 mos_M_12889 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_8 yrs_M_12981 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in inferolateral temporal cortex (area TEv, area 20)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
posterior (caudal) superior temporal cortex (area 22c)_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 posterior (caudal) superior temporal cortex (area 22c)_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. |
inferolateral temporal cortex (area TEv, area 20)_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 inferolateral temporal cortex (area TEv, area 20)_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. |
VZ in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in (rostral) midinferior temporal cortex (area 36) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in (rostral) midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in rostral midinferior temporal cortex (area 36) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in rostral midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
CP in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in CP in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in (rostral) midinferior temporal cortex (area 36) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in (rostral) midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in caudal midinferior temporal cortex (area TF) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
CP in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in rostral midinferior temporal cortex (area 36) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in rostral midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
polysensory temporal cortex (area 22p) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in polysensory temporal cortex (area 22p) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in inferolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in midinferior temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SZ in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in medial temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in temporal polar cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in midlateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in superolateral temporal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in lateral temporal-occipital cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Epilepsy, lateral temporal lobe, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, lateral temporal lobe, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Temporal Lobe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Temporal Lobe from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Familial Temporal Lobe, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset. |
Temporal Lobe Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Temporal Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
temporal arteritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease temporal arteritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
temporal lobe epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease temporal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
giant cell arteritis; ischemia; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease giant cell arteritis; ischemia; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe; seizures, febrile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe; sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe; sclerosis; seizures, febrile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; sclerosis; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
giant cell arteritis; polymyalgia rheumatica; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease giant cell arteritis; polymyalgia rheumatica; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epilepsy, temporal lobe; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temporal lobe epilepsy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temporal lobe epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
confusion; epilepsy, temporal lobe; sclerosis; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease confusion; epilepsy, temporal lobe; sclerosis; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; giant cell arteritis; polymyalgia rheumatica; rheumatoid arthritis; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; giant cell arteritis; polymyalgia rheumatica; rheumatoid arthritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
giant cell arteritis; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease giant cell arteritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
confusion; epilepsy, temporal lobe Gene SetFrom GAD Gene-Disease Associations genes associated with the disease confusion; epilepsy, temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temporal lobe Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temporal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term temporal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
superior temporal gyrus development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the superior temporal gyrus development biological process from the curated GO Biological Process Annotations 2015 dataset. |
Brain structure (temporal lobe volume) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Brain structure (temporal lobe volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
temporal lobe epilepsy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease temporal lobe epilepsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
temporal hypotrichosis Gene SetFrom HPO Gene-Disease Associations genes associated with the temporal hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the temporal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the temporal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Epilepsy, Temporal Lobe Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Temporal Lobe phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Temporal Arteritis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Temporal Arteritis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
temporal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal temporal bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal temporal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal temporal lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal temporal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small temporal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small temporal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal temporal memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal temporal memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epilepsy, familial temporal lobe, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
H3K27ac_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me3_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9me3_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me1_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me1_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27me3_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K36me3_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9ac_Brain Inferior Temporal Lobe Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9ac_Brain Inferior Temporal Lobe histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
temporal lobe Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue temporal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
temporal lobe Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue temporal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
superficial temporal vein Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue superficial temporal vein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
temporal lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
superficial temporal artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue superficial temporal artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medial temporal lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medial temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Lateral Temporal Lobe Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Lateral Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesial Temporal Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesial Temporal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neoplasm Of Temporal Lobe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of Temporal Lobe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Lobe Pleomorphic Xanthoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Lobe Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Familial Mesial Temporal Lobe Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Pallor Of Optic Disc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Pallor Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Epilepsy, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Epilepsy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Temporal Bone Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Temporal Bone Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Hypotrichosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Arteritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Arteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Temporal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eeg With Temporal Focal Spikes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Temporal Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Temporal Bossing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Temporal Bossing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
small temporal bone squamous part Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small temporal bone squamous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal bone squamous part morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal bone squamous part morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal bone tympanic part morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal bone tympanic part morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent temporal bone squamous part Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent temporal bone squamous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
temporal bone hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small temporal bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small temporal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
temporal bone squamous part hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal bone squamous part hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent temporal bone petrous part Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent temporal bone petrous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal bone petrous part morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal bone petrous part morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short temporal bone squamous part Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short temporal bone squamous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal bone zygomatic process morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal bone zygomatic process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent temporal bone zygomatic process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent temporal bone zygomatic process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal temporal lobe morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Oligodendrocyte precursor cell_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte precursor cell_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Astrocyte_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Astrocyte_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Chandelier cell_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Chandelier cell_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Oligodendrocyte_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Endothelial cell_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endothelial cell_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Microglial cell_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Microglial cell_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Neuron_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Neuron_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inhibitory neuron_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inhibitory neuron_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Excitatory neuron_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Excitatory neuron_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
GABAergic neuron_Middle temporal gyrus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the GABAergic neuron_Middle temporal gyrus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Familial temporal lobe epilepsy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial temporal lobe epilepsy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Temporal lobe epilepsy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Temporal lobe epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Temporal arteritis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Temporal arteritis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Temporal lobe epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Temporal lobe epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Temporal arteritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Temporal arteritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial temporal lobe epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Temporal lobe neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Temporal lobe neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Temporal lobe Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Temporal lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Temporal lobe Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Temporal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Temporal lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medial temporal lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medial temporal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Temporal gyrus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Temporal gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Middle temporal gyrus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Middle temporal gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inferior temporal gyrus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inferior temporal gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Superior temporal gyrus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Superior temporal gyrus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Superficial temporal artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Superficial temporal artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Superficial temporal vein Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Superficial temporal vein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Familial temporal lobe epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial temporal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MICAL1-related Lateral temporal epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MICAL1-related Lateral temporal epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Benign childhood epilepsy with centro-temporal spikes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left superior temporal gyrus thickness (schizophrenia interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left superior temporal gyrus thickness (schizophrenia interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Temporal lobe volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Temporal lobe volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Proportion of activated microglia (inferior temporal cortex) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proportion of activated microglia (inferior temporal cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Electrocardiogram morphology (amplitude at temporal datapoints) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Electrocardiogram morphology (amplitude at temporal datapoints) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Medial temporal lobe substructure volumes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Medial temporal lobe substructure volumes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mesial temporal lobe epilepsy with hippocampal sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mesial temporal lobe epilepsy with hippocampal sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Brain structure (temporal lobe volume) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain structure (temporal lobe volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Inferior temporal gyrus volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Inferior temporal gyrus volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Middle temporal gyrus volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle temporal gyrus volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Superior temporal gyrus volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Superior temporal gyrus volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Temporal pole volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Temporal pole volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Transverse temporal cortex volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Transverse temporal cortex volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lateral ventricle temporal horn volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lateral ventricle temporal horn volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Superior temporal sulcus banks volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Superior temporal sulcus banks volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dominant hereditary optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked myopathy with postural muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic Atrophy Type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital microvillous atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sveinsson Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy, Jerash type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy with respiratory distress 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset. |
Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset. |
Myopathy, X-Linked, With Postural Muscle Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset. |
Costeff optic atrophy syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy polyneuropathy deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Chorioretinal atrophy, progressive bifocal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
Gyrate Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset. |
Pigmented Paravenous Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
OPTIC ATROPHY 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
adult spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of prostate Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
juvenile spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intermediate spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
skin atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of testis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
partial optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
progressive muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
olivopontocerebellar atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
survival motor neuron spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gyrate atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
choroidal neovascularization; geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; metaplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroidal neovascularization; geographic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; prenatal exposure delayed effects; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic disc atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gyrate atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
geographic atrophy; macular degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blindness; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; choroidal neovascularization; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; aphasia; atrophy; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophy phenotype Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber; vision disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; amnesia; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; stomach atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; epilepsy; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy and moderate deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; huntington disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hippocampal atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonic disorders; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
skeletal muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
striated muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
MRI atrophy measures Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hippocampal atrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy 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. |
type 2 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
levator palpebrae superioris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral white matter atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy 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. |
atrophy/degeneration involving the corticospinal tracts Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized limb muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
global brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
caudate atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corpus callosum atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thenar muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skeletal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tongue atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
olivopontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dermal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripapillary chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subcortical cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse skin atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hand muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pelvic girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
leber optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral axonal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal pigment epithelial atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fundus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scapular muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the cerebrum Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
first dorsal interossei muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the caudate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy from cranial nerve compression Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar vermis atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
villous atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
iris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interosseus muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
type 1 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
superior rectus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
noninflammatory macular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized cerebral atrophy/hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limb-girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
testicular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peroneal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontotemporal cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Geographic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic atrophy 3-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dentatorubropallidoluysian atrophy Gene SetFrom KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset. |
ovary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle fiber atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cortex atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
testicular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney collecting duct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thymus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
brain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
optic nerve atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
retinal pigment epithelium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sebaceous gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midbrain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal tubule atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
seminal vesicle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal glomerulus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
meibomian gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreatic acinar cell atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
endometrium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epidermal atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iris atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vagina atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vulva atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
oviduct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
external male genitalia atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney medulla atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney papillary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy with progressive myoclonic epilepsy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, x-linked 2, infantile Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple system atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, x-linked, with postural muscle atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, jokela type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset. |
sveinsson choreoretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
scapuloperoneal spinal muscular atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, late-onset, finkel type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset. |
dentatorubro-pallidoluysian atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
{spinal muscular atrophy, type iii, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant 1, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
spastic paraplegia, optic atrophy, and neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 2, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
gyrate atrophy of choroid and retina with or without ornithinemia Gene SetFrom OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 3 with cataract Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neurodegeneration with optic atrophy, childhood onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal and bulbar muscular atrophy of kennedy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy plus syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
{leber optic atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |