Cataract, Age-Related Cortical, 1

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Results for "Cataract, Age-Related Cortical, 1": 815 gene sets

Name
Cataract, Age-Related Cortical, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset.
Parental longevity (mother's age at death or mother's attained age) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death or mother's attained age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cataract, Cortical, Juvenile-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.
posterior cortical cataract Gene Set From 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.
cortical cataract Gene Set From 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.
juvenile cortical cataract Gene Set From 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 Set From 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.
cortical pulverulent cataract Gene Set From 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.
Cortical Cataract Gene Set From 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.
Cortical, Lamellar, Or Zonular Nonsenile Cataract Gene Set From 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.
Cortical Pulverulent Cataract Gene Set From 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.
Dense Posterior Cortical Cataract Gene Set From 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 Set From 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 Set From 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.
cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
posterior cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cortical senile cataract Gene Set From 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.
Cortical pulverulent cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical pulverulent cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Occipital cortical area (total cortical area interaction) Gene Set From 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.
variable age at onset electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease variable age at onset electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
variable age at onset electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease variable age at onset electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
small for gestational age infant Gene Set From GAD Gene-Disease Associations genes associated with the disease small for gestational age infant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarche and menopause (age at onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease menarche and menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis (age of onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age and adiposity Gene Set From GAD Gene-Disease Associations genes associated with the disease age and adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age Gene Set From GAD Gene-Disease Associations genes associated with the disease age in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarche (age at onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease menarche (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age of menarche Gene Set From GAD Gene-Disease Associations genes associated with the disease age of menarche in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age at menarche/menopause Gene Set From GAD Gene-Disease Associations genes associated with the disease age at menarche/menopause in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age at first coronary bypass operation Gene Set From GAD Gene-Disease Associations genes associated with the disease age at first coronary bypass operation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease (age of onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age at natural menopause Gene Set From GAD Gene-Disease Associations genes associated with the disease age at natural menopause in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-associated memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease age-associated memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age at menarche Gene Set From GAD Gene-Disease Associations genes associated with the disease age at menarche in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menopause (age at onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-associated memory impairment (aami) Gene Set From GAD Gene-Disease Associations genes associated with the disease age-associated memory impairment (aami) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer by the age of 50 years Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer by the age of 50 years in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variable age at onset disease Gene Set From GAD Gene-Disease Associations genes associated with the disease variable age at onset disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
small for gestational age Gene Set From GAD Gene-Disease Associations genes associated with the disease small for gestational age in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term age in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
TP63_NULL MUTATION_GDS1434_308_mouse_Skin at embryonic age E18.5 Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the TP63_NULL MUTATION_GDS1434_308_mouse_Skin at embryonic age E18.5 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
CFTR_Deficiency_GDS1843_191_mouse_Lungs - Animals examined at 3 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CFTR_Deficiency_GDS1843_191_mouse_Lungs - Animals examined at 3 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
CFTR_Deficiency_GDS1843_192_mouse_Lungs - Animals examined at 6 weeks of age Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CFTR_Deficiency_GDS1843_192_mouse_Lungs - Animals examined at 6 weeks of age gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
age-dependent response to reactive oxygen species Gene Set From GO Biological Process Annotations 2015 genes participating in the age-dependent response to reactive oxygen species biological process from the curated GO Biological Process Annotations 2015 dataset.
age-dependent response to oxidative stress Gene Set From GO Biological Process Annotations 2015 genes participating in the age-dependent response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset.
Amyotrophic lateral sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Menarche and menopause (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Menarche and menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Alcohol dependence (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Menopause (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Blood pressure (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Menarche (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Femoral neck bone geometry and menarche (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (age of onset and psychomotor symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (age of onset and psychomotor symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age of smoking initiation Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age of smoking initiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Alzheimer's disease (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Alzheimer's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Narcolepsy (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Narcolepsy (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Parkinson's disease (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
middle age onset Gene Set From HPO Gene-Disease Associations genes associated with the middle age onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
marked delay in bone age Gene Set From HPO Gene-Disease Associations genes associated with the marked delay in bone age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysharmonic bone age Gene Set From HPO Gene-Disease Associations genes associated with the dysharmonic bone age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
accelerated bone age after puberty Gene Set From HPO Gene-Disease Associations genes associated with the accelerated bone age after puberty phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large for gestational age Gene Set From HPO Gene-Disease Associations genes associated with the large for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small for gestational age Gene Set From HPO Gene-Disease Associations genes associated with the small for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
{menopause, natural, age at, qtl2} Gene Set From OMIM Gene-Disease Associations genes associated with the {menopause, natural, age at, qtl2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menarche, age at, qtl3} Gene Set From OMIM Gene-Disease Associations genes associated with the {menarche, age at, qtl3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{bulimia nervosa, age of onset of weight loss in} Gene Set From OMIM Gene-Disease Associations genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menopause, natural, age at, qtl3} Gene Set From OMIM Gene-Disease Associations genes associated with the {menopause, natural, age at, qtl3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menopause, natural, age at, qtl1} Gene Set From OMIM Gene-Disease Associations genes associated with the {menopause, natural, age at, qtl1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menarche, age at, qtl2} Gene Set From OMIM Gene-Disease Associations genes associated with the {menarche, age at, qtl2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menarche, age at, qtl} Gene Set From OMIM Gene-Disease Associations genes associated with the {menarche, age at, qtl} phenotype from the curated OMIM Gene-Disease Associations dataset.
{menopause, natural, age at, qtl4} Gene Set From OMIM Gene-Disease Associations genes associated with the {menopause, natural, age at, qtl4} phenotype from the curated OMIM Gene-Disease Associations dataset.
AGE/RAGE pathway(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the AGE/RAGE pathway(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Age-Associated Memory Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Associated Memory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Bone Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Age At Menarche Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Age At Menarche in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Large For Gestational Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large For Gestational Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small For Gestational Age (Disorder) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small For Gestational Age (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small For Gestational Age Fetus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small For Gestational Age Fetus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Advanced Bone Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Age At Menopause Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Age At Menopause in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Middle Age Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Middle Age Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Accelerated Bone Age After Puberty Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Accelerated Bone Age After Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infant, Small For Gestational Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infant, Small For Gestational Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Marked Delay In Bone Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Marked Delay In Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysharmonic Bone Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysharmonic Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetus Small For Gestational Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetus Small For Gestational Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Poor Visual Behavior For Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Visual Behavior For Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Age-associated B cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Age-associated B cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
AGE RAGE pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the AGE RAGE pathway pathway from the WikiPathways Pathways 2024 dataset.
Variable age at onset electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Variable age at onset electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Variable age at onset electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Variable age at onset electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature and advanced bone age Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature and advanced bone age phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Small for gestational age Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Small for gestational age phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early age onset of sporadic thoracic aortic dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adverse response to inhaled corticosteroid treatment x age interaction in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adverse response to inhaled corticosteroid treatment x age interaction in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Allergic disease (asthma, hay fever and/or eczema) (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at first birth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at first birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer disease and age of onset Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer disease and age of onset phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Glucocorticoid-induced osteonecrosis (age 10 years and older) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glucocorticoid-induced osteonecrosis (age 10 years and older) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease (familial, age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (familial, age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gestational age at birth (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (spine) and age at menarche Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (spine) and age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bone mineral density (hip) and age at menarche Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (hip) and age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Menarche (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at voice drop Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at voice drop phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Extrinsic epigenetic age acceleration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Extrinsic epigenetic age acceleration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Intrinsic epigenetic age acceleration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intrinsic epigenetic age acceleration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Menopause (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Machado-Joseph disease (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Machado-Joseph disease (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at adiposity rebound Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at adiposity rebound phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age spots Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age spots phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease (onset at age over 80) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease (onset at age over 80) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Spherical equivalent or myopia (age of diagnosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spherical equivalent or myopia (age of diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Frontotemporal dementia with GRN mutation (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Frontotemporal dementia with GRN mutation (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Frontotemporal dementia (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Frontotemporal dementia (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Huntington's disease (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Huntington's disease (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Glioblastoma (age-stratified) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glioblastoma (age-stratified) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Leisure-time exercise behaviour (age-stratified) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Leisure-time exercise behaviour (age-stratified) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Type 1 diabetes (age at diagnosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 1 diabetes (age at diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
perceptual and visual search speed (trail making test A) (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the perceptual and visual search speed (trail making test A) (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alcohol dependence (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Blood pressure (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease (age at diagnosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (age at diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body size at age 10 Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body size at age 10 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder (age of onset and psychotic symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder (age of onset and psychotic symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardiovascular risk factors (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular risk factors (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Amyotrophic lateral sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Amyotrophic lateral sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at smoking initiation in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at smoking initiation in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lean body mass and age at menarche (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lean body mass and age at menarche (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neuroticism (age interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuroticism (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Menarche and menopause (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Menarche and menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Femoral neck bone geometry and menarche (age at onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early age at menarche Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
diarrhoeal disease at age 1 Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the diarrhoeal disease at age 1 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
diarrhoeal disease at age 1 with doctor diagnosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the diarrhoeal disease at age 1 with doctor diagnosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
diarrhoeal disease at age 2 Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the diarrhoeal disease at age 2 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
diarrhoeal disease at age 2 with doctor diagnosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the diarrhoeal disease at age 2 with doctor diagnosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at first sexual intercourse Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at first sexual intercourse phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Smoking behaviour (age at first cigarette) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Smoking behaviour (age at first cigarette) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relative brain age Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relative brain age phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Polycystic ovary syndrome (adjusted for age) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (adjusted for age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Polycystic ovary syndrome (adjusted for age and BMI) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polycystic ovary syndrome (adjusted for age and BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (age <50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age <50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index x age interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index x age interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (age <50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (age <50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (age >50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (age >50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (age>50) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (age>50) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index x sex x age interaction (4df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index x sex x age interaction (4df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (combined parental attained age, Martingale residuals) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (combined parental attained age, Martingale residuals) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (mother's age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (mother's attained age) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's attained age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (father's age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (father's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (father's attained age) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (father's attained age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (combined parental age at death) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (combined parental age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gait speed in old age Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gait speed in old age phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Type 2 diabetes (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gestational age at birth (child effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth (child effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epigenetic age acceleration in alcohol use disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epigenetic age acceleration in alcohol use disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Longevity (age >90th survival percentile) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Longevity (age >90th survival percentile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Longevity (age >99th survival percentile) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Longevity (age >99th survival percentile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at suicide Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at suicide phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at menarche Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at menarche phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe coronary stenosis (young age of onset interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe coronary stenosis (young age of onset interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
AGE-RAGE signaling pathway in diabetic complications Gene Set From KEGG Pathways 2026 proteins participating in the AGE-RAGE signaling pathway in diabetic complications pathway from the KEGG Pathways 2026 dataset.
PMC9541747-AGE-53-680-s003.xlsx-TableS6-Table_S6_Genes_with_missense_mutations_in_Yaroslavl_cattle_MAF_0_1_and_FST_0_4_in_the_1000_Bull_Genomes_Run_9_MAF Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC9541747-AGE-53-680-s003.xlsx-TableS6-Table_S6_Genes_with_missense_mutations_in_Yaroslavl_cattle_MAF_0_1_and_FST_0_4_in_the_1000_Bull_Genomes_Run_9_MAF transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC4682820-pgen.1005734.s010.xls-Age-regulated_STAT1_targets-List_of_age-regulated_STAT1_ChIP-seq_targets_STAT1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC4682820-pgen.1005734.s010.xls-Age-regulated_STAT1_targets-List_of_age-regulated_STAT1_ChIP-seq_targets_STAT1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC4682820-pgen.1005734.s010.xls-Age-regulated_STAT3_targets-List_of_age-regulated_STAT3_ChIP-seq_targets_STAT3 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC4682820-pgen.1005734.s010.xls-Age-regulated_STAT3_targets-List_of_age-regulated_STAT3_ChIP-seq_targets_STAT3 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_1_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_1_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_2_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_2_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_3_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_3_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_4_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_4_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_5_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_5_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_6_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_6_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_8_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_8_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_9_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_9_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_10_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_10_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_11_MSC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC6070530-41398_2018_200_MOESM3_ESM.xlsx-regional_cluster_PFC-MSC-age-bin_11_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, posterior polar, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, posterior polar, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zonular pulverulent cataract 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zonular pulverulent cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 15, multiple types Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant, multiple types, with microcornea Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, nuclear total Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, nuclear total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperferritinemia cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Absent corpus callosum cataract immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Absent corpus callosum cataract immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, zonular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, zonular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, membranous Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, membranous phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Posterior polar cataract type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Posterior polar cataract type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Cataract, Nuclear Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.
Cataract, Central Saccular, With Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Central Saccular, With Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Cataract, posterior polar, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 4 from the curated CTD Gene-Disease Associations dataset.
Cataract, posterior polar, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 3 from the curated CTD Gene-Disease Associations dataset.
Cerulean cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerulean cataract from the curated CTD Gene-Disease Associations dataset.
Cataract, Zonular Pulverulent 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Zonular Pulverulent 3 from the curated CTD Gene-Disease Associations dataset.
Cataract, Zonular Pulverulent 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Zonular Pulverulent 1 from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
Absent corpus callosum cataract immunodeficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Absent corpus callosum cataract immunodeficiency from the curated CTD Gene-Disease Associations dataset.
CATARACT 32, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Zonular, with Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
CATARACT 6, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.
Anterior polar cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anterior polar cataract 2 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive Congenital 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant, Multiple Types 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.
Cataract microcornea syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract microcornea syndrome from the curated CTD Gene-Disease Associations dataset.
Cataract, zonular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, zonular from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.
CATARACT 3, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract, congenital, with microcornea or slight microphthalmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, congenital, with microcornea or slight microphthalmia from the curated CTD Gene-Disease Associations dataset.
Cataract, Pulverulent, Juvenile-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 2 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 1 from the curated CTD Gene-Disease Associations dataset.
CATARACT 4, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract, Coppock-Like Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Coppock-Like from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.
CATARACT, CONGENITAL OR JUVENILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.
CATARACT 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 23 from the curated CTD Gene-Disease Associations dataset.
cataract Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cataract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
morgagni cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease morgagni cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
immature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease immature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
posterior polar cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital nuclear cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital nuclear cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; exfoliation syndrome; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; exfoliation syndrome; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
zonular pulverulent cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease zonular pulverulent cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant coral-like cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract, presenile Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract, presenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cataract in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cataract Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cataract in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cataract Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cataract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
anterior polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the anterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile cataract Gene Set From HPO Gene-Disease Associations genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cataract Gene Set From HPO Gene-Disease Associations genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulverulent cataract Gene Set From HPO Gene-Disease Associations genes associated with the pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sutural cataract Gene Set From HPO Gene-Disease Associations genes associated with the sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
iridescent posterior subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the iridescent posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
total cataract Gene Set From HPO Gene-Disease Associations genes associated with the total cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerulean cataract Gene Set From HPO Gene-Disease Associations genes associated with the cerulean cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate cataract Gene Set From HPO Gene-Disease Associations genes associated with the punctate cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior y-sutural cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior y-sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
zonular cataract Gene Set From HPO Gene-Disease Associations genes associated with the zonular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
membranous cataract Gene Set From HPO Gene-Disease Associations genes associated with the membranous cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the diffuse nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cataract Gene Set From HPO Gene-Disease Associations genes associated with the cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lamellar cataract Gene Set From HPO Gene-Disease Associations genes associated with the lamellar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cataract Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cataract phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cataract 5, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 36 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, juvenile, with microcornea and glucosuria Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, juvenile, with microcornea and glucosuria phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 40, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 40, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 9, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract with late-onset corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia, high, with cataract and vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 30, pulverulent Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 30, pulverulent phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 22, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 22, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, cataract, retinitis pigmentosa, and sperm abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, cataract, retinitis pigmentosa, and sperm abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 3, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract 41 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract 41 phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract 42 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract 42 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 1, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 29, coralliform Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 29, coralliform phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 20, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 33 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 33 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 14, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 12, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 39, multiple types, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperferritinemia-cataract syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hyperferritinemia-cataract syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 34, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, pulverulent or cerulean, with or without microcornea Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 6, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 2, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 16, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 15, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 3 with cataract Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
adult i phenotype without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, syndromic Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, syndromic phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 18, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 17, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 25 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 23 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 27, nuclear progressive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 4, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 31, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 10, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
anterior segment anomalies with or without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 38, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 38, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia with cataract 2 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia with cataract 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia with cataract 1 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia with cataract 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 13 with adult i phenotype Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 13 with adult i phenotype phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 35, congenital nuclear Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 35, congenital nuclear phenotype from the curated OMIM Gene-Disease Associations dataset.
Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
After-Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease After-Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuclear Non-Senile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuclear Non-Senile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonnuclear Polymorphic Congenital Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonnuclear Polymorphic Congenital Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Total Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Total Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Induced Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Induced Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Lamellar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Lamellar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Presenile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Presenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Embryonal Nuclear Cataract (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Embryonal Nuclear Cataract (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuclear Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuclear Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sutural Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Morgagnian Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Morgagnian Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Posterior Polar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Membranous Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Membranous Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mature Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mature Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coralliform Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coralliform Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crystalline Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Crystalline Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Corpus Callosum Cataract Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absent Corpus Callosum Cataract Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies With Or Without Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies With Or Without Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Branchiootorenal Syndrome With Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Branchiootorenal Syndrome With Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lamellar Pulverulent Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lamellar Pulverulent Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Capsular Cataract (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Capsular Cataract (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atopic Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atopic Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Punctate Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Punctate Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticosteroid Induced Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticosteroid Induced Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Incipient Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Incipient Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Type Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Type Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Polar Cataract 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Polar Cataract 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Nuclear Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Nuclear Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Polar Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iridescent Posterior Subcapsular Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iridescent Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Capsular Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Capsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Y-Sutural Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Y-Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nuclear cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nuclear cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
developmental cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the developmental cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
total cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the total cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
posterior subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior polar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior polar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lamellar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lamellar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
polar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the polar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
mature cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mature cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sutural cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sutural cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
immature cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the immature cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cataract Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the cataract phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Cataract Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cataract from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
hyperferritinemia-cataract syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease hyperferritinemia-cataract syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hyperferritinemia-cataract syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hyperferritinemia-cataract syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 9 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 9 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polar cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Morgagni cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Morgagni cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Immature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 8 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 8 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 6 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 6 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 1 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 1 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 32 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 32 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 13 with adult i phenotype Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 13 with adult i phenotype in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 4 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 4 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 11 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 11 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 10 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 10 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 3 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 3 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 21 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 21 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 31 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 31 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nuclear senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nuclear senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myotonic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 14 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 14 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 34 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 34 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tetanic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tetanic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 12 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 12 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 1 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 1 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aculeiform cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aculeiform cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 4 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 4 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 3 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 3 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 9 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 9 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Porencephaly-microcephaly-bilateral congenital cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Porencephaly-microcephaly-bilateral congenital cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 16 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 16 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 39 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 39 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 14 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 14 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 15 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 15 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 10 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 10 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 34 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 34 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 11 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 11 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Zonular Pulverulent Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Zonular Pulverulent Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 6 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 6 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 13 with adult I phenotype Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 13 with adult I phenotype phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 5 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 5 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 21 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 21 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nuclear cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nuclear cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 22 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 22 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 19 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 19 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 17 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 17 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nuclear pulverulent cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nuclear pulverulent cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 20 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 20 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 31 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 31 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile cataract-microcornea-renal glucosuria syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile cataract-microcornea-renal glucosuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 46 juvenile-onset Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 46 juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset anterior polar cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset anterior polar cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical subplate Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cortical granule Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins in the Kir4.1-dystrophin complex, cortical astrocytes protein complex from the CORUM Protein Complexes dataset.
Focal cortical dysplasia of Taylor Gene Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Malformations of Cortical Development Gene Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperostosis, Cortical, Congenital from the curated CTD Gene-Disease Associations dataset.
cortical blindness Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
posterior cortical atrophy Gene Set From 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.
cortical surface area Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
cerebellar cortical atrophy Gene Set From 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.
abnormal cortical bone morphology Gene Set From 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 thickening of long bone diaphyses Gene Set From 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.
frontal cortical atrophy Gene Set From 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.
cortical irregularity Gene Set From 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 Set From 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 Set From 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 Set From 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.
diaphyseal cortical sclerosis Gene Set From 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 Set From HPO Gene-Disease Associations genes associated with the cortical visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral cortical atrophy Gene Set From 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 microcysts Gene Set From 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 Set From 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 Set From 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 atrophy Gene Set From 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.
renal cortical cysts Gene Set From 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.
temporal cortical atrophy Gene Set From 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.
Malformations of Cortical Development Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical dysplasia-focal epilepsy syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal cortical carcinoma Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal cortical carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset.
cortical Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Cerebral Cortical Atrophy Gene Set From 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.
Adrenal Cortical Adenoma Gene Set From 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 Set From 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.
Cerebral Cortical Hemiatrophy Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Frontal Cortical Atrophy Gene Set From 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.
Temporal Cortical Atrophy Gene Set From 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.
Cerebellar Cortical Atrophy Gene Set From 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.
Cerebellar Cortical Dysplasia Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Posterior Cortical Atrophy Syndrome Gene Set From 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.
Cortical Displasia Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Focal Cortical Dysplasia Of Taylor Gene Set From 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.
Renal Cortical Atrophy Gene Set From 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 Set From 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 Set From 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.
Isolated Focal Cortical Dysplasia Gene Set From 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 Set From 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 Set From 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 Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortical Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cortical Gyral Simplification Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Cerebral Cortical Neurodegeneration Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cortical renal glomerulopathies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cortical ventricular zone morphology Gene Set From 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 Set From 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 Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized cortical plate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cortical intermediate zone morphology Gene Set From 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.
ectopic cortical neuron Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Reactome Pathways 2024 proteins participating in the Regulation of cortical dendrite branching pathway from the Reactome Pathways 2024 dataset.
cortical actin cytoskeleton organization Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Complex cortical dysplasia with other brain malformations Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical tubers phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical dysplasia Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Focal cortical dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral cortical atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical thickness (MOSTest) Gene Set From 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 Set From 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 Set From 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 Set From 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.
Posterior cortical atrophy and Alzheimer's disease Gene Set From 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.
Cingulate cortical amyloid beta load Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cortical surface area (visual PC2) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cortical surface area (global PC1) Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.

Harmonizome 3.0

Cataract, Age-Related Cortical, 1 Gene Set

Parental longevity (mother's age at death or mother's attained age) Gene Set

Cataract, Cortical, Juvenile-Onset Gene Set

posterior cortical cataract Gene Set

cortical cataract Gene Set

juvenile cortical cataract Gene Set

dense posterior cortical cataract Gene Set

cortical pulverulent cataract Gene Set

Cortical Cataract Gene Set

Cortical, Lamellar, Or Zonular Nonsenile Cataract Gene Set

Cortical Pulverulent Cataract Gene Set

Dense Posterior Cortical Cataract Gene Set

Anterior Cortical Cataract Gene Set

Posterior Cortical Cataract Gene Set

cortical cataract Gene Set

anterior cortical cataract Gene Set

posterior cortical cataract Gene Set

Cortical senile cataract Gene Set

Cortical pulverulent cataract Gene Set

Occipital cortical area (total cortical area interaction) Gene Set

variable age at onset electroclinical syndrome Gene Set

variable age at onset electroclinical syndrome Gene Set

small for gestational age infant Gene Set

menarche and menopause (age at onset) Gene Set

multiple sclerosis (age of onset) Gene Set

age and adiposity Gene Set

age Gene Set

menarche (age at onset) Gene Set

age of menarche Gene Set

age at menarche/menopause Gene Set

age at first coronary bypass operation Gene Set

parkinson's disease (age of onset) Gene Set

age at natural menopause Gene Set

age-associated memory impairment Gene Set

age at menarche Gene Set

menopause (age at onset) Gene Set

age-associated memory impairment (aami) Gene Set

breast cancer by the age of 50 years Gene Set

variable age at onset disease Gene Set

small for gestational age Gene Set

age Gene Set

SCA1_Knock-in_GDS1756_233_mouse_Forebrain tissue - 4 weeks of age Gene Set

TP63_NULL MUTATION_GDS1434_308_mouse_Skin at embryonic age E18.5 Gene Set

SCA1_Knock-in_GDS1756_231_mouse_Cerebellum tissue - 4 weeks of age Gene Set

SCA1_Knock-in_GDS1756_232_mouse_Cerebellum tissue - 12 weeks of age Gene Set

SCA1_Knock-in_GDS1756_234_mouse_Forebrain tissue - 12 weeks of age Gene Set

CFTR_Deficiency_GDS1843_191_mouse_Lungs - Animals examined at 3 weeks of age Gene Set

CFTR_Deficiency_GDS1843_192_mouse_Lungs - Animals examined at 6 weeks of age Gene Set

age-dependent response to reactive oxygen species Gene Set

age-dependent response to oxidative stress Gene Set

Amyotrophic lateral sclerosis (age of onset) Gene Set

Menarche and menopause (age at onset) Gene Set

Alcohol dependence (age at onset) Gene Set

Menopause (age at onset) Gene Set

Blood pressure (age interaction) Gene Set

Menarche (age at onset) Gene Set

Femoral neck bone geometry and menarche (age at onset) Gene Set

Bipolar disorder (age of onset and psychomotor symptoms) Gene Set

Age of smoking initiation Gene Set

Alzheimer's disease (age of onset) Gene Set

Narcolepsy (age of onset) Gene Set

Multiple sclerosis (age of onset) Gene Set

Parkinson's disease (age of onset) Gene Set

middle age onset Gene Set

marked delay in bone age Gene Set

dysharmonic bone age Gene Set

accelerated bone age after puberty Gene Set

large for gestational age Gene Set

small for gestational age Gene Set

{menopause, natural, age at, qtl2} Gene Set

{menarche, age at, qtl3} Gene Set

{bulimia nervosa, age of onset of weight loss in} Gene Set

{menopause, natural, age at, qtl3} Gene Set

{menopause, natural, age at, qtl1} Gene Set

{menarche, age at, qtl2} Gene Set

{menarche, age at, qtl} Gene Set

{menopause, natural, age at, qtl4} Gene Set

AGE/RAGE pathway(Homo sapiens) Gene Set

Age-Associated Memory Impairment Gene Set