mild cognitive impairment

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Results for "mild cognitive impairment": 399 gene sets

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Mild Cognitive Impairment Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mild Cognitive Impairment from the curated CTD Gene-Disease Associations dataset.
mild cognitive impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease mild cognitive impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Mild cognitive impairment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mild cognitive impairment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cognitive decline rate in late mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive decline rate in late mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Rate of cognitive decline in mild cognitive impairment (time interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rate of cognitive decline in mild cognitive impairment (time interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal volume in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal volume in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (immediate recall) in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (immediate recall) in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal AB1-42 levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal AB1-42 levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal fluid t-tau levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid t-tau levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal fluid p-tau levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid p-tau levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild Cognitive Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Cognitive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cognitive impairment, vascular stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive impairment, vascular stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive impairment; alzheimers disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive impairment; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive impairment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cognitive impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cognitive impairment Gene Set From HPO Gene-Disease Associations genes associated with the cognitive impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cognitive impairment with or without cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
Vascular Cognitive Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Cognitive Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Impairment With Or Without Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cognitive impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Language delay and attention deficit-hyperactivity disorder/cognitive impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Language delay and attention deficit-hyperactivity disorder/cognitive impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cognitive impairment in depression Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive impairment in depression phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypotension and cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypotension and cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
cognitive impairment (MMSE score) in Parkinson’s disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the cognitive impairment (MMSE score) in Parkinson’s disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive impairment test score Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive impairment test score phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
mild hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mild hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild neurosensory hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mild neurosensory hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mild Neurosensory Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Neurosensory Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Impairment Level: Total Impairment Of Both Eyes (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Impairment Level: Total Impairment Of Both Eyes (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Delirium, Dementia, Amnestic, Cognitive Disorders from the curated CTD Gene-Disease Associations dataset.
COGNITIVE FUNCTION 1, SOCIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COGNITIVE FUNCTION 1, SOCIAL from the curated CTD Gene-Disease Associations dataset.
cognitive disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cognitive disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cognitive disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cognitive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cognitive decline Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive decline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive ability Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive ability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function; motor function Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function; motor function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early cognitive decline Gene Set From GAD Gene-Disease Associations genes associated with the disease early cognitive decline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive reactivity Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive reactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive performance Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive performance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive test performance Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive test performance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; cognitive function Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; cognitive function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function and diabetes Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function and diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function in children Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function in children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive trait Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive function in older men Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive function in older men in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive ability ; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive ability ; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cognitive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Cognitive decline (age-related) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cognitive decline (age-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cognitive decline Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cognitive decline phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cognitive test performance Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cognitive test performance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Alzheimer's disease (cognitive decline) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Alzheimer's disease (cognitive decline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cognitive performance Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cognitive performance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cognitive function Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cognitive function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
cognitive disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cognitive disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Cognitive Therapy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cognitive Therapy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Delirium, Dementia, Amnestic, Cognitive Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cognitive Reserve Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cognitive Reserve phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cognitive Deterioration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv-1-Associated Cognitive Motor Complex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv-1-Associated Cognitive Motor Complex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Cognitive Decline Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Cognitive Decline in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cognitive Affective Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cognitive Affective Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postoperative Cognitive Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Cognitive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cognitive Changes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cognitive Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cognitive inflexibility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cognitive inflexibility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cognitive disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cognitive disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cognitive disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cognitive disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cognitive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cognitive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subjective cognitive decline Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subjective cognitive decline in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood-onset motor and cognitive regression syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Parkinson's disease progression (cognitive) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease progression (cognitive) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive function Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
General cognitive ability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the General cognitive ability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive flexibility Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive flexibility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive performance in schizophrenia or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive performance in schizophrenia or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to cognitive-behavioural therapy in anxiety and major depressive disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in anxiety and major depressive disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to cognitive-behavioural therapy in anxiety disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in anxiety disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to cognitive-behavioural therapy in major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive decline (age-related) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive decline (age-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive decline Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive decline phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive function in longevity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive function in longevity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive test performance Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive test performance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease (cognitive decline) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease (cognitive decline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive performance Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive performance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Dimensional psychopathology (Cognitive) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dimensional psychopathology (Cognitive) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive ability (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive ability (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive ability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive ability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Verbal cognitive ability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Verbal cognitive ability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Numerical cognitive ability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Numerical cognitive ability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Figural/spatial cognitive ability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Figural/spatial cognitive ability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (global cognition) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (global cognition) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (executive function) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (executive function) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (language) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (language) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (memory) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (memory) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive performance (processing speed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive performance (processing speed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (visuospatial skill) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (visuospatial skill) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related cognitive decline (attention/processing speed) (slope of z-scores) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related cognitive decline (attention/processing speed) (slope of z-scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Metachromatic leukodystrophy, mild Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metachromatic leukodystrophy, mild phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensorineural deafness with mild renal dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUCOPOLYSACCHARIDOSIS, TYPE VI, MILD Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, MILD phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MONONEUROPATHY OF THE MEDIAN NERVE, MILD Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MONONEUROPATHY OF THE MEDIAN NERVE, MILD from the curated CTD Gene-Disease Associations dataset.
Osteoarthritis with Mild Chondrodysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteoarthritis with Mild Chondrodysplasia from the curated CTD Gene-Disease Associations dataset.
mild pre-eclampsia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mild pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mild chondrodysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild chondrodysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild phenotype xeroderma pigmentosum Gene Set From GAD Gene-Disease Associations genes associated with the disease mild phenotype xeroderma pigmentosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild osteogenesis imperfecta Gene Set From GAD Gene-Disease Associations genes associated with the disease mild osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild and severe substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease mild and severe substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild hyperhomocysteinaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild hyperhomocysteinaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild myotubular myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mild myotubular myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild hdn Gene Set From GAD Gene-Disease Associations genes associated with the disease mild hdn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild ehlers-danlos syndrome type iv Gene Set From GAD Gene-Disease Associations genes associated with the disease mild ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild dyslipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild dyslipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild gestational diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease mild gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild homocystinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease mild homocystinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mild in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mild postnatal growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild intrauterine growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild short stature Gene Set From HPO Gene-Disease Associations genes associated with the mild short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, mild Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, mild phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild proteinuria Gene Set From HPO Gene-Disease Associations genes associated with the mild proteinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
maple syrup urine disease, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the maple syrup urine disease, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
brachyolmia 4 with mild epiphyseal and metaphyseal changes Gene Set From OMIM Gene-Disease Associations genes associated with the brachyolmia 4 with mild epiphyseal and metaphyseal changes phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, mild, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, mild, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, mild, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
mononeuropathy of the median nerve, mild Gene Set From OMIM Gene-Disease Associations genes associated with the mononeuropathy of the median nerve, mild phenotype from the curated OMIM Gene-Disease Associations dataset.
osteoarthritis with mild chondrodysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the osteoarthritis with mild chondrodysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
[hyperphenylalaninemia, non-pku mild] Gene Set From OMIM Gene-Disease Associations genes associated with the [hyperphenylalaninemia, non-pku mild] phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.
sensorineural deafness with mild renal dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
Mild Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Expressive Language Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Bronchopulmonary Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Bronchopulmonary Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Non-Proliferative Diabetic Retinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Non-Proliferative Diabetic Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Hereditary Factor Viii Deficiency Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maroteaux-Lamy Syndrome, Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maroteaux-Lamy Syndrome, Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Citrullinemia, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Citrullinemia, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Mood Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Mood Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorineural Deafness With Mild Renal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Steroid 21-Hydroxylase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Steroid 21-Hydroxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Fetal Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Fetal Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hunter'S Syndrome, Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hunter'S Syndrome, Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mcardle Disease, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mcardle Disease, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Hypermetropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Hypermetropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mononeuropathy Of The Median Nerve, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mononeuropathy Of The Median Nerve, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Postnatal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Canavan Disease, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Canavan Disease, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Proteinuria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Proteinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Microcephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Intrauterine Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Eczema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Eczema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Dysmorphic Features Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Dysmorphic Features in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Myopia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Apparent Mineralocorticoid Excess, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apparent Mineralocorticoid Excess, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Delay, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Dysmorphism, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Dysmorphism, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Adverse Event Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Adverse Event in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Thrombocytopenia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Splenomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Splenomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Radial Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Radial Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
H139Hfs13* PPM1K causes a mild variant of MSUD Gene Set From Reactome Pathways 2024 proteins participating in the H139Hfs13* PPM1K causes a mild variant of MSUD pathway from the Reactome Pathways 2024 dataset.
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual disability-severe speech delay-mild dysmorphism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mild pre-eclampsia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mild pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent mild asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent mild asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mild non-PKU hyperphenylalanemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild non-PKU hyperphenylalanemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild hyperphenylalaninemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild hyperphenylalaninemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild Canavan disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild Canavan disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild hemophilia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild hemophilia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-severe speech delay-mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild proteinuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild proteinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild macrothrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild macrothrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the CV-A6-associated hand, foot, and mouth disease (severe vs mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild influenza (H1N1) infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild influenza (H1N1) infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hematuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hematuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Glucosuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glucosuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proteinuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proteinuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ketonuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ketonuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erosive tooth wear (severe vs none or mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erosive tooth wear (severe vs none or mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild to moderate chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild to moderate chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of malaria infection (mild or asymptomatic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of malaria infection (mild or asymptomatic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of mild malaria attacks Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of mild malaria attacks phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild obesity-related type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild obesity-related type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild age-related type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild age-related type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hearing impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, cochlear, with myopia and intellectual impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SPECIFIC LANGUAGE IMPAIRMENT 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 2 from the curated CTD Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
SPECIFIC LANGUAGE IMPAIRMENT 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 3 from the curated CTD Gene-Disease Associations dataset.
Age-Related Hearing Impairment 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Age-Related Hearing Impairment 1 from the curated CTD Gene-Disease Associations dataset.
Specific Language Impairment 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Specific Language Impairment 4 from the curated CTD Gene-Disease Associations dataset.
SPECIFIC LANGUAGE IMPAIRMENT 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 1 from the curated CTD Gene-Disease Associations dataset.
hearing impairment; hearing loss; otosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; otosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; blood pressure, arterial; memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing impairment; hearing loss; hearing loss, high-frequency Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multidimensional impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease multidimensional impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory impairment, subjective Gene Set From GAD Gene-Disease Associations genes associated with the disease memory impairment, subjective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anticholinergic challenge-induced memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease anticholinergic challenge-induced memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
human spermatogenesis impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease human spermatogenesis impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing impairment; hearing loss; infant, premature, diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic diseases, inborn; hearing impairment; hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; lipids; memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; lipids; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness; hearing impairment; hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss 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.
hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spermatogenic impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease spermatogenic impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms 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.
hearing impairment; hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic hearing impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic hearing impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
impairment Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term impairment in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Parent of origin effect on language impairment (paternal) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parent of origin effect on language impairment (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related hearing impairment (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related hearing impairment (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related hearing impairment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hearing impairment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
neurological speech impairment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the neurological speech impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
memory impairment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the memory impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
language impairment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the language impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hearing impairment Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hearing impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal seizures with impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures with impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the bilateral sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
high-frequency hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the high-frequency hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures without impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
low-frequency sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the low-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
language impairment Gene Set From HPO Gene-Disease Associations genes associated with the language impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensory impairment Gene Set From HPO Gene-Disease Associations genes associated with the sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
memory impairment Gene Set From HPO Gene-Disease Associations genes associated with the memory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the congenital sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prelingual sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the prelingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postlingual sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the postlingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the bilateral conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
profound hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the profound hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive pulmonary function impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive pulmonary function impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal sensory impairment of all modalities Gene Set From HPO Gene-Disease Associations genes associated with the distal sensory impairment of all modalities 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.
childhood onset sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neurological speech impairment Gene Set From HPO Gene-Disease Associations genes associated with the neurological speech impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
high-frequency sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the high-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mixed hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the severe sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adult onset sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the adult onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impairment of galactose metabolism Gene Set From HPO Gene-Disease Associations genes associated with the impairment of galactose metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal sensory impairment Gene Set From HPO Gene-Disease Associations genes associated with the distal sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impairment of fructose metabolism Gene Set From HPO Gene-Disease Associations genes associated with the impairment of fructose metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
profound sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the profound sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual impairment Gene Set From HPO Gene-Disease Associations genes associated with the visual impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensorineural hearing impairment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sensorineural hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
conductive hearing impairment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the conductive hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nonsyndromic hearing impairment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nonsyndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
syndromic hearing impairment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the syndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mental retardation with language impairment and autistic features Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation with language impairment and autistic features phenotype from the curated OMIM Gene-Disease Associations dataset.
?microtia, hearing impairment, and cleft palate (ar) Gene Set From OMIM Gene-Disease Associations genes associated with the ?microtia, hearing impairment, and cleft palate (ar) phenotype from the curated OMIM Gene-Disease Associations dataset.
specific language impairment qtl, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the specific language impairment qtl, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
specific language impairment qtl, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the specific language impairment qtl, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
{specific language impairment 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {specific language impairment 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{memory impairment, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {memory impairment, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
?microtia with or without hearing impairment (ad) Gene Set From OMIM Gene-Disease Associations genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.
{age-related hearing impairment 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {age-related hearing impairment 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
specific language impairment qtl, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the specific language impairment qtl, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{age-related hearing impairment 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {age-related hearing impairment 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
{specific language impairment 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {specific language impairment 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
Severe Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations 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.
Central Visual Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complex Partial Seizure With Impairment Of Consciousness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complex Partial Seizure With Impairment Of Consciousness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prelingual Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prelingual Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midface Hypoplasia, Hearing Impairment, Elliptocytosis, And Nephrocalcinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midface Hypoplasia, Hearing Impairment, Elliptocytosis, And Nephrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short-Term Memory Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short-Term Memory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Specific Language Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Specific Language Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Onset Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
High-Frequency Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Frequency Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosocial Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosocial Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Impairment Of Attention Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Impairment Of Attention in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia With Or Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia With Or Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia, Hearing Impairment, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia, Hearing Impairment, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vision Impairment And Blindness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vision Impairment And Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Semantic Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Semantic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Syntactic Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Syntactic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Memory Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Sensory Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderate Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Sensorineural Hearing Impairment 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.
Hepatic Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Communication Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Communication Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impairment Of Urinary Concentration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impairment Of Urinary Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Sensory Impairment Of All Modalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment Of All Modalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impairment Of Activities Of Daily Living Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impairment Of Activities Of Daily Living in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postlingual Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postlingual Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impairment, Light Touch Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impairment, Light Touch Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gross Motor Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gross Motor Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impairment Of Galactose Metabolism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impairment Of Galactose Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Onset Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Moderate Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pulmonary Function Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pulmonary Function Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Speech Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Speech Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Visual Impairment And Blindness (Excl Colour Blindness) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visual Impairment And Blindness (Excl Colour Blindness) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unilateral Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unilateral Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Low-Frequency Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-Frequency Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Expressive Language Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expressive Language Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
conductive hearing impairment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the conductive hearing impairment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
syndromic hearing impairment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the syndromic hearing impairment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nonsyndromic hearing impairment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nonsyndromic hearing impairment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sensorineural hearing impairment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sensorineural hearing impairment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Chronic hyperglycemia impairment of neuron function Gene Set From WikiPathways Pathways 2024 proteins participating in the Chronic hyperglycemia impairment of neuron function pathway from the WikiPathways Pathways 2024 dataset.
Specific language impairment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Specific language impairment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with speech impairment and dysmorphic facies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with speech impairment and dysmorphic facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Conductive hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Conductive hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Prelingual sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Prelingual sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bilateral conductive hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bilateral conductive hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bilateral sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bilateral sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Memory impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Memory impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-Syndromic Hereditary Hearing Impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-Syndromic Hereditary Hearing Impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ocular impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ocular impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral visual impairment and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral visual impairment and intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Moderate sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Moderate sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Specific language impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Specific language impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurocognitive impairment in HIV-1 infection (continuous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neurocognitive impairment in HIV-1 infection (continuous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neurocognitive impairment in HIV-1 infection (dichotomous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neurocognitive impairment in HIV-1 infection (dichotomous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (asymptomatic neurocogntive impairment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (asymptomatic neurocogntive impairment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related hearing impairment (low/mid frequency) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related hearing impairment (low/mid frequency) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related hearing impairment (high frequency) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related hearing impairment (high frequency) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Language impairment in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Language impairment in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related hearing impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parent of origin effect on language impairment (paternal) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parent of origin effect on language impairment (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reading disability or specific language impairment (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reading disability or specific language impairment (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hearing impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Mild Cognitive Impairment Gene Set

mild cognitive impairment Gene Set

Mild cognitive impairment Gene Set

Cognitive decline rate in late mild cognitive impairment Gene Set

Rate of cognitive decline in mild cognitive impairment (time interaction) Gene Set

Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) Gene Set

Hippocampal volume in mild cognitive impairment Gene Set

Logical memory (immediate recall) in mild cognitive impairment Gene Set

Logical memory (delayed recall) in mild cognitive impairment Gene Set

Cerebrospinal AB1-42 levels in mild cognitive impairment Gene Set

Cerebrospinal fluid t-tau levels in mild cognitive impairment Gene Set

Cerebrospinal fluid p-tau levels in mild cognitive impairment Gene Set

Mild Cognitive Disorder Gene Set

Cognitive impairment with or without cerebellar ataxia Gene Set

cognitive impairment, vascular stroke, ischemic Gene Set

cognitive impairment; alzheimers disease Gene Set

cognitive impairment Gene Set

cognitive impairment Gene Set

cognitive impairment Gene Set

cognitive impairment with or without cerebellar ataxia Gene Set

Vascular Cognitive Impairment Gene Set

Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia Gene Set

Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set

Cognitive impairment Gene Set

Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome Gene Set

Language delay and attention deficit-hyperactivity disorder/cognitive impairment Gene Set

Cognitive impairment in depression Gene Set

Hypotension and cognitive impairment Gene Set

cognitive impairment (MMSE score) in Parkinson’s disease Gene Set

Cognitive impairment test score Gene Set

mild hearing impairment Gene Set

mild neurosensory hearing impairment Gene Set

Mild Neurosensory Hearing Impairment Gene Set

Mild Hearing Impairment Gene Set

Mild Conductive Hearing Impairment Gene Set

HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) Gene Set

Impairment Level: Total Impairment Of Both Eyes (Disorder) Gene Set

Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set

COGNITIVE FUNCTION 1, SOCIAL Gene Set

cognitive disorder Gene Set

cognitive disorder Gene Set

cognitive disorder Gene Set

cognitive decline Gene Set

cognitive ability Gene Set

cognitive function; motor function Gene Set

cognitive function Gene Set

early cognitive decline Gene Set

cognitive reactivity Gene Set

cognitive performance Gene Set

cognitive test performance Gene Set

alzheimer's disease; cognitive function Gene Set

cognitive function and diabetes Gene Set

cognitive function in children Gene Set

cognitive trait Gene Set

cognitive function in older men Gene Set

cognitive ability ; hypertension Gene Set

cognitive Gene Set

Cognitive decline (age-related) Gene Set

Cognitive decline Gene Set

Cognitive test performance Gene Set

Alzheimer's disease (cognitive decline) Gene Set

Cognitive performance Gene Set

Cognitive function Gene Set

cognitive disorder Gene Set

Cognitive Therapy Gene Set

Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set

Cognitive Reserve Gene Set

Cognitive Deterioration Gene Set

Hiv-1-Associated Cognitive Motor Complex Gene Set

Age-Related Cognitive Decline Gene Set

Cerebellar Cognitive Affective Syndrome Gene Set

Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set

Postoperative Cognitive Dysfunction Gene Set

Cognitive Changes Gene Set

cognitive inflexibility Gene Set

Cognitive disorder Gene Set

Cognitive disorder Gene Set

Cognitive disorder Gene Set

Subjective cognitive decline Gene Set