Continuous Spike And Waves During Slow Sleep

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Results for "Continuous Spike And Waves During Slow Sleep": 1002 gene sets

Name
Continuous Spike And Waves During Slow Sleep Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Continuous Spike And Waves During Slow Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Continuous spike and waves during slow sleep Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Continuous spike and waves during slow sleep phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
eeg with centrotemporal focal spike waves Gene Set From HPO Gene-Disease Associations genes associated with the eeg with centrotemporal focal spike waves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with focal spike waves Gene Set From HPO Gene-Disease Associations genes associated with the eeg with focal spike waves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Eeg With Focal Spike Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Spike Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Centrotemporal Focal Spike Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Centrotemporal Focal Spike Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Sharp Slow Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Sharp Slow Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Continuous Slow Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Continuous Slow Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Obstructive sleep apnea (average oxygen saturation during sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea (average oxygen saturation during sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea during REM sleep (apnea hypopnea index) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea during REM sleep (apnea hypopnea index) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
fatigue; sleep disorders; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep disorders; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased slow-wave sleep duration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased slow-wave sleep duration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal slow-wave sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal slow-wave sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
RHO GTPases Activate WASPs and WAVEs Gene Set From Reactome Pathways 2024 proteins participating in the RHO GTPases Activate WASPs and WAVEs pathway from the Reactome Pathways 2024 dataset.
Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eeg With Irregular Generalized Spike And Wave Complexes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Irregular Generalized Spike And Wave Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
sleep apnea, obstructive; sleep deprivation Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea, obstructive; sleep deprivation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
Sleep duration (short sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (short sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (long sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (long sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Brain Waves Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Brain Waves in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
low amplitude p300 waves Gene Set From GAD Gene-Disease Associations genes associated with the disease low amplitude p300 waves in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
waves Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term waves in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Brain Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Emg Positive Sharp Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Emg Positive Sharp Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Focal Sharp Waves Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Focal Sharp Waves in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
continuous performance task Gene Set From GAD Gene-Disease Associations genes associated with the disease continuous performance task in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
continuous Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term continuous in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Continuous Muscle Fiber Activity, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Continuous Muscle Fiber Activity, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Continuous Leakage Of Urine Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Continuous Leakage Of Urine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Continuous Tremor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Continuous Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Continuous Electrocardiogram Sinus Bradycardia (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Continuous Electrocardiogram Sinus Bradycardia (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Continuous Electrocardiogram - Paroxysmal Supraventricular Tachycardia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Continuous Electrocardiogram - Paroxysmal Supraventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Response to lithium treatment in bipolar disorder (continuous phenotype) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lithium treatment in bipolar disorder (continuous phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Insomnia complaints (continuous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Insomnia complaints (continuous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) phenotype in GWAS datasets from the GWAS Catalog SNP-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.
Bipolar disorder lithium response (continuous) or schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder lithium response (continuous) or schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Number of stillbirths in continuous marriage Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Number of stillbirths in continuous marriage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Degraded stimulus continuous performance test score Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Degraded stimulus continuous performance test score phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
transition between fast and slow fiber Gene Set From GO Biological Process Annotations 2015 genes participating in the transition between fast and slow fiber biological process from the curated GO Biological Process Annotations 2015 dataset.
transition between slow and fast fiber Gene Set From GO Biological Process Annotations 2015 genes participating in the transition between slow and fast fiber biological process from the curated GO Biological Process Annotations 2015 dataset.
transition between fast and slow fiber Gene Set From GO Biological Process Annotations 2023 genes participating in the transition between fast and slow fiber biological process from the curated GO Biological Process Annotations 2023 dataset.
transition between fast and slow fiber Gene Set From GO Biological Process Annotations 2025 genes participating in the transition between fast and slow fiber biological process from the curated GO Biological Process Annotations 2025 dataset.
spike Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spike in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
eeg with spike-wave complexes (>3.5 hz) Gene Set From HPO Gene-Disease Associations genes associated with the eeg with spike-wave complexes (>3.5 hz) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with spike-wave complexes Gene Set From HPO Gene-Disease Associations genes associated with the eeg with spike-wave complexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal spike wave discharge Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spike wave discharge phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spike Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spike in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Eeg With Spike-Wave Complexes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Spike-Wave Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Spike-Wave Complexes (2.5-3.5 Hz) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Spike-Wave Complexes (2.5-3.5 Hz) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Spike-Wave Complexes (>3.5 Hz) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Spike-Wave Complexes (>3.5 Hz) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal spike wave discharge Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spike wave discharge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Downregulation of ACE2 by SARS CoV 2 spike protein Gene Set From WikiPathways Pathways 2024 proteins participating in the Downregulation of ACE2 by SARS CoV 2 spike protein pathway from the WikiPathways Pathways 2024 dataset.
Maturation of spike protein_9683686 Gene Set From Reactome Pathways 2024 proteins participating in the Maturation of spike protein_9683686 pathway from the Reactome Pathways 2024 dataset.
Maturation of spike protein_9694548 Gene Set From Reactome Pathways 2024 proteins participating in the Maturation of spike protein_9694548 pathway from the Reactome Pathways 2024 dataset.
Spike Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spike in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Type I interferon induction and signaling during SARS CoV 2 infection Gene Set From WikiPathways Pathways 2024 proteins participating in the Type I interferon induction and signaling during SARS CoV 2 infection pathway from the WikiPathways Pathways 2024 dataset.
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set From Reactome Pathways 2024 proteins participating in the FBXL7 down-regulates AURKA during mitotic entry and in early mitosis pathway from the Reactome Pathways 2024 dataset.
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection Gene Set From Reactome Pathways 2024 proteins participating in the RNA Pol II CTD phosphorylation and interaction with CE during HIV infection pathway from the Reactome Pathways 2024 dataset.
Sleep Initiation and Maintenance Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.
fatigue; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
total energy intake and cytokine sleep factors Gene Set From GAD Gene-Disease Associations genes associated with the disease total energy intake and cytokine sleep factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Initiation and Maintenance Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation And Maintenance Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation And Maintenance Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
hs4 enhancer complex (slow migrating complex) Gene Set From CORUM Protein Complexes proteins in the hs4 enhancer complex (slow migrating complex) protein complex from the CORUM Protein Complexes dataset.
Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenic syndrome, congenital, postsynaptic slow-channel from the curated CTD Gene-Disease Associations dataset.
slow coronary flow Gene Set From GAD Gene-Disease Associations genes associated with the disease slow coronary flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
slow Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term slow in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
slow endocytic recycling Gene Set From GO Biological Process Annotations 2015 genes participating in the slow endocytic recycling biological process from the curated GO Biological Process Annotations 2015 dataset.
slow-twitch skeletal muscle fiber contraction Gene Set From GO Biological Process Annotations 2015 genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2015 dataset.
eeg with abnormally slow frequencies Gene Set From HPO Gene-Disease Associations genes associated with the eeg with abnormally slow frequencies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow saccadic eye movements Gene Set From HPO Gene-Disease Associations genes associated with the slow saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow-growing hair Gene Set From HPO Gene-Disease Associations genes associated with the slow-growing hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with generalized slow activity Gene Set From HPO Gene-Disease Associations genes associated with the eeg with generalized slow activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow decrease in visual acuity Gene Set From HPO Gene-Disease Associations genes associated with the slow decrease in visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis leading to amputation due to slow healing fractures Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow progression Gene Set From HPO Gene-Disease Associations genes associated with the slow progression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slow postnatal weight gain Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow postnatal weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
slow aging Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow aging phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
slow extinction of fear memory Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow extinction of fear memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
slow wallerian degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow wallerian degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myasthenic syndrome, slow-channel congenital Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, slow-channel congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
{aids, slow progression to} Gene Set From OMIM Gene-Disease Associations genes associated with the {aids, slow progression to} phenotype from the curated OMIM Gene-Disease Associations dataset.
[acetylation, slow] Gene Set From OMIM Gene-Disease Associations genes associated with the [acetylation, slow] phenotype from the curated OMIM Gene-Disease Associations dataset.
slow muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue slow muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
slow twitch muscle fiber Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue slow twitch muscle fiber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
slow muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue slow muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Muscle-slow muscle cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Muscle-slow muscle cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Slow Channel Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slow Channel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slow Acetylator Due To N-Acetyltransferase Enzyme Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slow Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eeg With Multifocal Slow Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Multifocal Slow Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow Progression Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Progression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow-Growing Hair Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow-Growing Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Osteomyelitis Leading To Amputation Due To Slow Healing Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteomyelitis Leading To Amputation Due To Slow Healing Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow Decrease In Visual Acuity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Decrease In Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow-Flow Phenomenon Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow-Flow Phenomenon in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Slow Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Slow Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Abnormally Slow Frequencies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Abnormally Slow Frequencies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow Pupillary Light Response Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow Pupillary Light Response in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slow-Growing Nails Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow-Growing Nails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of slow-twitch skeletal muscle fiber contraction Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.
slow endocytic recycling Gene Set From GO Biological Process Annotations 2023 genes participating in the slow endocytic recycling biological process from the curated GO Biological Process Annotations 2023 dataset.
slow-twitch skeletal muscle fiber contraction Gene Set From GO Biological Process Annotations 2023 genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.
slow axonal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the slow axonal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
slow postnatal weight gain Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow postnatal weight gain phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow Wallerian degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow Wallerian degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow aging Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow aging phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow extinction of fear memory Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow extinction of fear memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow movement Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
regulation of slow-twitch skeletal muscle fiber contraction Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.
slow endocytic recycling Gene Set From GO Biological Process Annotations 2025 genes participating in the slow endocytic recycling biological process from the curated GO Biological Process Annotations 2025 dataset.
slow-twitch skeletal muscle fiber contraction Gene Set From GO Biological Process Annotations 2025 genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.
Slow muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Slow muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Slow muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Slow muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Slow twitch muscle fiber Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Slow twitch muscle fiber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Slow-Channel Congenital Myasthenia Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Slow-Channel Congenital Myasthenia Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Factor B fast/slow polymorphism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Factor B fast/slow polymorphism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
joint destruction in rheumatoid arthritis (rapid vs slow) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the joint destruction in rheumatoid arthritis (rapid vs slow) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
the co-stimulatory signal during t-cell activation Gene Set From Biocarta Pathways proteins participating in the the co-stimulatory signal during t-cell activation pathway from the Biocarta Pathways dataset.
regulation of p27 phosphorylation during cell cycle progression Gene Set From Biocarta Pathways proteins participating in the regulation of p27 phosphorylation during cell cycle progression pathway from the Biocarta Pathways dataset.
RC complex during S-phase of cell cycle Gene Set From CORUM Protein Complexes proteins in the RC complex during S-phase of cell cycle protein complex from the CORUM Protein Complexes dataset.
RC complex during G2/M-phase of cell cycle Gene Set From CORUM Protein Complexes proteins in the RC complex during G2/M-phase of cell cycle protein complex from the CORUM Protein Complexes dataset.
fear during childbirth Gene Set From GAD Gene-Disease Associations genes associated with the disease fear during childbirth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vasodilation during pregnancy Gene Set From GAD Gene-Disease Associations genes associated with the disease vasodilation during pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Gata-6_KO_GDS4782_330_mouse_Adult heart during pressure overload Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Gata-6_KO_GDS4782_330_mouse_Adult heart during pressure overload gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Gata-4_KO_GDS4782_329_mouse_Adult heart during pressure overload Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Gata-4_KO_GDS4782_329_mouse_Adult heart during pressure overload gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
midbrain-hindbrain boundary maturation during brain development Gene Set From GO Biological Process Annotations 2015 genes participating in the midbrain-hindbrain boundary maturation during brain development biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during bundle of his cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during bundle of his cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription during meiosis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription during meiosis biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription from rna polymerase ii promoter during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of transcription from rna polymerase ii promoter during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription from rna polymerase ii promoter during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
maintenance of transcriptional fidelity during dna-templated transcription elongation Gene Set From GO Biological Process Annotations 2015 genes participating in the maintenance of transcriptional fidelity during dna-templated transcription elongation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during av node cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during av node cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane repolarization during sa node cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane repolarization during sa node cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription during meiosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription during meiosis biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane repolarization during bundle of his cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane repolarization during bundle of his cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during purkinje myocyte cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during purkinje myocyte cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during sa node cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during sa node cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription during mitosis Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription during mitosis biological process from the curated GO Biological Process Annotations 2015 dataset.
membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2015 genes participating in the membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
maintenance of transcriptional fidelity during dna-templated transcription elongation from rna polymerase ii promoter Gene Set From GO Biological Process Annotations 2015 genes participating in the maintenance of transcriptional fidelity during dna-templated transcription elongation from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
increased serum bile acid concentration during pregnancy Gene Set From HPO Gene-Disease Associations genes associated with the increased serum bile acid concentration during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal liver function tests during pregnancy Gene Set From HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
elevated serum transaminases during infections Gene Set From HPO Gene-Disease Associations genes associated with the elevated serum transaminases during infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired mammary gland growth during pregnancy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mammary gland growth during lactation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland growth during lactation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome pairing during meiosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome pairing during meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
persistence of medial edge epithelium during palatal shelf fusion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the persistence of medial edge epithelium during palatal shelf fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
embryonic lethality during organogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the embryonic lethality during organogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mammary gland growth during pregnancy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality during organogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality during organogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial embryonic lethality during organogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial embryonic lethality during organogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal dna methylation during gametogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal dna methylation during gametogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
meiotic nondisjunction during m1 phase Gene Set From MPO Gene-Phenotype Associations gene mutations causing the meiotic nondisjunction during m1 phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal x-y chromosome synapsis during male meiosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal x-y chromosome synapsis during male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Association of TriC/CCT with target proteins during biosynthesis Gene Set From Reactome Pathways 2014 proteins participating in the Association of TriC/CCT with target proteins during biosynthesis pathway from the Reactome Pathways dataset.
Cyclin A/B1 associated events during G2/M transition Gene Set From Reactome Pathways 2014 proteins participating in the Cyclin A/B1 associated events during G2/M transition pathway from the Reactome Pathways dataset.
Cyclin E associated events during G1/S transition Gene Set From Reactome Pathways 2014 proteins participating in the Cyclin E associated events during G1/S transition pathway from the Reactome Pathways dataset.
Abnormal Liver Function Tests During Pregnancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Liver Function Tests During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Increased Serum Bile Acid Concentration During Pregnancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Serum Bile Acid Concentration During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Elevated Serum Transaminases During Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Serum Transaminases During Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pain During Injection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain During Injection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Alcohol Consumption During Pregnancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
membrane depolarization during AV node cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during AV node cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during SA node cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during SA node cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane repolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane repolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during bundle of His cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during bundle of His cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during SA node cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during SA node cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane repolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane repolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during bundle of His cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during bundle of His cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during Purkinje myocyte cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during Purkinje myocyte cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
membrane depolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the membrane depolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II Gene Set From GO Biological Process Annotations 2023 genes participating in the maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
promoter clearance during DNA-templated transcription Gene Set From GO Biological Process Annotations 2023 genes participating in the promoter clearance during DNA-templated transcription biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
maintenance of transcriptional fidelity during transcription elongation Gene Set From GO Biological Process Annotations 2023 genes participating in the maintenance of transcriptional fidelity during transcription elongation biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic lethality during organogenesis, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality during organogenesis, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality during organogenesis, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality during organogenesis, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mammary gland growth during pregnancy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mammary gland growth during lactation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland growth during lactation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
persistence of medial edge epithelium during palatal shelf fusion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the persistence of medial edge epithelium during palatal shelf fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality during organogenesis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality during organogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal DNA methylation during gametogenesis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal DNA methylation during gametogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
meiotic nondisjunction during M1 phase Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the meiotic nondisjunction during M1 phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal X-Y chromosome synapsis during male meiosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synapsis during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired mammary gland growth during pregnancy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature mammary gland growth during pregnancy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal X-Y chromosome synaptonemal complex assembly during male meiosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synaptonemal complex assembly during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
T cell antigen receptor TCR pathway during Staphylococcus aureus infection Gene Set From WikiPathways Pathways 2024 proteins participating in the T cell antigen receptor TCR pathway during Staphylococcus aureus infection pathway from the WikiPathways Pathways 2024 dataset.
Selective expression of chemokine receptors during T cell polarization Gene Set From WikiPathways Pathways 2024 proteins participating in the Selective expression of chemokine receptors during T cell polarization pathway from the WikiPathways Pathways 2024 dataset.
Neural crest cell migration during development Gene Set From WikiPathways Pathways 2024 proteins participating in the Neural crest cell migration during development pathway from the WikiPathways Pathways 2024 dataset.
Activation of HOX genes during differentiation Gene Set From Reactome Pathways 2024 proteins participating in the Activation of HOX genes during differentiation pathway from the Reactome Pathways 2024 dataset.
Activation of anterior HOX genes in hindbrain development during early embryogenesis Gene Set From Reactome Pathways 2024 proteins participating in the Activation of anterior HOX genes in hindbrain development during early embryogenesis pathway from the Reactome Pathways 2024 dataset.
Association of TriC/CCT with target proteins during biosynthesis Gene Set From Reactome Pathways 2024 proteins participating in the Association of TriC/CCT with target proteins during biosynthesis pathway from the Reactome Pathways 2024 dataset.
Chromatin modifications during the maternal to zygotic transition (MZT) Gene Set From Reactome Pathways 2024 proteins participating in the Chromatin modifications during the maternal to zygotic transition (MZT) pathway from the Reactome Pathways 2024 dataset.
Cyclin A/B1/B2 associated events during G2/M transition Gene Set From Reactome Pathways 2024 proteins participating in the Cyclin A/B1/B2 associated events during G2/M transition pathway from the Reactome Pathways 2024 dataset.
Cyclin E associated events during G1/S transition Gene Set From Reactome Pathways 2024 proteins participating in the Cyclin E associated events during G1/S transition pathway from the Reactome Pathways 2024 dataset.
Epithelial-Mesenchymal Transition (EMT) during gastrulation Gene Set From Reactome Pathways 2024 proteins participating in the Epithelial-Mesenchymal Transition (EMT) during gastrulation pathway from the Reactome Pathways 2024 dataset.
TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation Gene Set From Reactome Pathways 2024 proteins participating in the TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation pathway from the Reactome Pathways 2024 dataset.
membrane depolarization during AV node cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during AV node cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during SA node cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during SA node cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane repolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane repolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during bundle of His cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during bundle of His cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during SA node cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during SA node cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane repolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane repolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane depolarization during action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane depolarization during action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane repolarization during action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane repolarization during action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during bundle of His cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during bundle of His cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during Purkinje myocyte cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during Purkinje myocyte cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
membrane depolarization during atrial cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the membrane depolarization during atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of membrane depolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II Gene Set From GO Biological Process Annotations 2025 genes participating in the maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
promoter clearance during DNA-templated transcription Gene Set From GO Biological Process Annotations 2025 genes participating in the promoter clearance during DNA-templated transcription biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of membrane repolarization during cardiac muscle cell action potential Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
maintenance of transcriptional fidelity during transcription elongation Gene Set From GO Biological Process Annotations 2025 genes participating in the maintenance of transcriptional fidelity during transcription elongation biological process from the curated GO Biological Process Annotations 2025 dataset.
Abnormal liver function tests during pregnancy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal liver function tests during pregnancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypersomnia during a major depressive episode in bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypersomnia during a major depressive episode in bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Caudate activity during reward Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Caudate activity during reward phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Activity variability during wake Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Activity variability during wake phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pain medicine use during menstruation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pain medicine use during menstruation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Opioid requirements during laparoscopic-assisted colectomy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Opioid requirements during laparoscopic-assisted colectomy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
T wave morphology restitution during exercise (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the T wave morphology restitution during exercise (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
T wave morphology restitution during exercise Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the T wave morphology restitution during exercise phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
T wave morphology restitution during recovery from exercise Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the T wave morphology restitution during recovery from exercise phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
T wave morphology restitution during recovery from exercise (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the T wave morphology restitution during recovery from exercise (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Phenylephrine infusion rate during anesthesia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Phenylephrine infusion rate during anesthesia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depression x maternal smoking during pregnancy interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression x maternal smoking during pregnancy interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety x maternal smoking during pregnancy interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety x maternal smoking during pregnancy interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sleep Deprivation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Deprivation from the curated CTD Gene-Disease Associations dataset.
Sleep Apnea, Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea, Obstructive from the curated CTD Gene-Disease Associations dataset.
Sleep Apnea Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea Syndromes from the curated CTD Gene-Disease Associations dataset.
REM Sleep Behavior Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.
Sleep Bruxism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Bruxism from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders, Circadian Rhythm from the curated CTD Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders from the curated CTD Gene-Disease Associations dataset.
Sleep Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Sleep in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sleep disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
advanced sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypertension; inflammation; obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; inflammation; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed sleep phase syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep duration Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep duration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep deprivation Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep deprivation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders, circadian rhythm Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders, circadian rhythm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed sleep phase syndrome. Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; fatigue; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; fatigue; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; sleep apnea, obstructive; snoring Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; sleep apnea, obstructive; snoring in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hot flashes; osteoporosis, postmenopausal; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hot flashes; osteoporosis, postmenopausal; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep-disordered breathing Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep-disordered breathing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; schizophrenia; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; blood pressure, arterial; sleep apnea Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; neoplasms; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; neoplasms; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercapnic respiratory failure; hypoventilation; sleep apnea, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd; sleep Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd; sleep in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstructive sleep apnea syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease obstructive sleep apnea syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term sleep in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Obstructive sleep apnea_Hepatic Tissue_GSE1873 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Obstructive sleep apnea_Hepatic Tissue_GSE1873 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle process Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle process biological process from the curated GO Biological Process Annotations 2015 dataset.
sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
Sleep time Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep depth Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep depth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep quality Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep quality phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep-related phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sleep disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sleep disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sleep-wake cycle disturbance Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sleep-wake cycle disturbance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sleep disturbance Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sleep disturbance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
obstructive sleep apnea Gene Set From HPO Gene-Disease Associations genes associated with the obstructive sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sleep-wake cycle disturbance Gene Set From HPO Gene-Disease Associations genes associated with the sleep-wake cycle disturbance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sleep disturbance Gene Set From HPO Gene-Disease Associations genes associated with the sleep disturbance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sleep apnea Gene Set From HPO Gene-Disease Associations genes associated with the sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal rapid eye movement (rem) sleep Gene Set From HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Circadian Rhythm phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Deprivation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Deprivation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Arousal Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Arousal Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea, Obstructive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Obstructive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea, Central Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
REM Sleep Behavior Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the REM Sleep Behavior Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Bruxism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Bruxism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep, REM Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep, REM phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Stages Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Stages phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders, Intrinsic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Intrinsic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal paradoxical sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sleep behavior Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sleep behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fragmentation of sleep/wake states Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fragmentation of sleep/wake states phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
advanced sleep phase syndrome, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{delayed sleep phase syndrome, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {delayed sleep phase syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
[respiratory rhythmicity in sleep] Gene Set From OMIM Gene-Disease Associations genes associated with the [respiratory rhythmicity in sleep] phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep-phase syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Advanced Sleep Phase Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep Phase Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Sleep Phase Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-24 Hour Sleep-Wake Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-24 Hour Sleep-Wake Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonorganic Sleep Wake Cycle Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonorganic Sleep Wake Cycle Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Shift-Work Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Shift-Work Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Bruxism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Bruxism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Sleep Apnea Hypopnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Sleep Apnea Hypopnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Disordered Breathing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Disordered Breathing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction 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.
Obstructive Sleep Apnea Hypopnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Sleep Apnea Hypopnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rem Sleep Behavior Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rem Sleep Behavior Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Related Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Related Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Sleep Phase Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Pediatric Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Pediatric Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Onset Of Sleep Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Onset Of Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Airway Resistance Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Resistance Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Attack Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Attack in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insufficient Sleep Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insufficient Sleep Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adjustment Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adjustment Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Environmental Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Environmental Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limit-Setting Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limit-Setting Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Disorders, Extrinsic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Disorders, Extrinsic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Related Painful Erections Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Related Painful Erections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duration Of Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duration Of Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Disturbances Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Disturbances in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
[D]Sleep Disturbances (& [Hypersomnia] Or [Insomnia]) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype [D]Sleep Disturbances (& [Hypersomnia] Or [Insomnia]) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Wake Cycle Disturbance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Wake Cycle Disturbance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Deprivation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Deprivation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rem Sleep Deprivation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rem Sleep Deprivation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Related Neurogenic Tachypnea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Related Neurogenic Tachypnea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Onset Latency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Onset Latency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Advanced Sleep Phase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Sleep Phase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Rapid Eye Movement Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Rapid Eye Movement Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Sleep Phase Disorder, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Sleep Phase Disorder, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fragmented Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fragmented Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Restless Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restless Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Onset Insomnia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Onset Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Non-Organic Sleep Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Non-Organic Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Fragmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Fragmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Wake Inversion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Wake Inversion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep duration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep duration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal circadian sleep/wake cycle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circadian sleep/wake cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal paradoxical sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fragmentation of sleep/wake states Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fragmentation of sleep/wake states phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep behavior Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep behavior phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep behavior Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal sleep behavior phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Sleep regulation Gene Set From WikiPathways Pathways 2024 proteins participating in the Sleep regulation pathway from the WikiPathways Pathways 2024 dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
Sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sleep disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep apnea Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sleep apnea in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive sleep apnea Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Obstructive sleep apnea in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
REM sleep behavior disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease REM sleep behavior disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Delayed sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Delayed sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-hypotonia-spasticity-sleep disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sleep apnea Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sleep apnea 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.
Familial sleep-related hypermotor epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sleep-related hypermotor epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Advanced sleep phase syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Advanced sleep phase syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep traits (multi-trait analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep traits (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (oversleepers vs undersleepers) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (oversleepers vs undersleepers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea trait (apnea hypopnea index) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea trait (apnea hypopnea index) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea trait (average respiratory event duration) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea trait (average respiratory event duration) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Night sleep phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Night sleep phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Daytime sleep phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Daytime sleep phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (> 10 hours) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (> 10 hours) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1/2-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1/2-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep start time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep start time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1/3-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1/3-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep end time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep end time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep activity levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep activity levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea (BMI adjusted) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea (BMI adjusted) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep-related phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep quality Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep quality phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep latency Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep latency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depressive symptom (sleep problems) (binary trait) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depressive symptom (sleep problems) (binary trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (number of episodes) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (number of episodes) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations 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.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome 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.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multicentric osteolysis, nodulosis and arthropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, short stature, and impaired glucose metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy dilated with woolly hair and keratoderma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone fragility with contractures, arterial rupture, and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulna and fibula absence of with severe limb deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor v and factor viii, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary Paragangliomas and Pheochromocytomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Band-like calcification with simplified gyration and polymicrogyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monocyte and dendritic cell deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined malonic and methylmalonic aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniosynostosis and dental anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, hyperphagia, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebroretinal microangiopathy with calcifications and cysts Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, normal intelligence and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Calcification of joints and arteries Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pineal hyperplasia AND diabetes mellitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Morbid obesity and spermatogenic failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of factor V and factor VIII, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Camptodactyly, tall stature, and hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne 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.
Growth deficiency and mental retardation with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy 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.
Combined deficiency of sialidase AND beta galactosidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mrna cleavage and polyadenylation specificity factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
collagen and cuticulin-based cuticle extracellular matrix part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
mitochondrial sorting and assembly machinery complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set From CORUM Protein Complexes proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set From CORUM Protein Complexes proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.
6S methyltransferase and RG-containing Sm proteins complex Gene Set From CORUM Protein Complexes proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.
Remodeling and spacing factor (RSF) complex Gene Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Nucleic and chromatin Fanconi complex Gene Set From CORUM Protein Complexes proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Prime and Bond NT Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.
drospirenone and ethinyl estradiol combination Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.
Hypophosphatemic Rickets And Hyperparathyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.
Combined Cellular And Humoral Immune Defects With Granulomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema 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.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.
Craniosynostosis, anal anomalies, and porokeratosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.
Classical Lissencephalies and Subcortical Band Heterotopias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Signs and Symptoms, Digestive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.
Head and Neck Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms 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.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.
Postoperative Nausea and Vomiting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.
Hypopituitarism and septooptic 'dysplasia' Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset.
Aplasia of Lacrimal and Salivary Glands Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.
Calcification of Joints and Arteries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset.
CHOANAL ATRESIA AND LYMPHEDEMA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset.
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.
Asthma, Nasal Polyps, And Aspirin Intolerance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.
Neoplasms, Germ Cell and Embryonal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.
Cutis Gyrata Syndrome of Beare And Stevenson Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Wounds and Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset.
Schizophrenia and Disorders with Psychotic Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset.
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset.
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.
Hereditary Breast and Ovarian Cancer Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset.
Keratosis palmoplantaris with periodontopathia and onychogryposis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia and onychogryposis from the curated CTD Gene-Disease Associations dataset.
Intracranial Embolism and Thrombosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset.
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset.
Nevi and Melanomas Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nevi and Melanomas from the curated CTD Gene-Disease Associations dataset.
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy dilated with Woolly hair and keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset.
Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.
Mullerian Aplasia and Hyperandrogenism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Esophageal and Gastric Varices Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal and Gastric Varices from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
Carcinoma, squamous cell of head and neck Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head and neck from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
Extravasation of Diagnostic and Therapeutic Materials Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic and Therapeutic Materials from the curated CTD Gene-Disease Associations dataset.
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Knuckle pads, leuconychia and sensorineural deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia and sensorineural deafness from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset.
Hyperekplexia and Epilepsy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Iris hypoplasia and glaucoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.
Sarcoma family syndrome of Li and Fraumeni Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset.
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa and Deafness from the curated CTD Gene-Disease Associations dataset.
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.
Lipoid Proteinosis of Urbach and Wiethe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach and Wiethe from the curated CTD Gene-Disease Associations dataset.
Hypertelorism with esophageal abnormality and hypospadias Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
Jervell And Lange-Nielsen Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jervell And Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Neoplasms, Glandular and Epithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Glandular and Epithelial from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Continuous Spike And Waves During Slow Sleep Gene Set

Continuous spike and waves during slow sleep Gene Set

eeg with centrotemporal focal spike waves Gene Set

eeg with focal spike waves Gene Set

Eeg With Focal Spike Waves Gene Set

Eeg With Centrotemporal Focal Spike Waves Gene Set

Eeg With Focal Sharp Slow Waves Gene Set

Eeg With Continuous Slow Activity Gene Set

Obstructive sleep apnea (average oxygen saturation during sleep) Gene Set

Obstructive sleep apnea during REM sleep (apnea hypopnea index) Gene Set

fatigue; sleep disorders; sleep initiation and maintenance disorders Gene Set

decreased slow-wave sleep duration Gene Set

abnormal slow-wave sleep pattern Gene Set

RHO GTPases Activate WASPs and WAVEs Gene Set

Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) Gene Set

Eeg With Irregular Generalized Spike And Wave Complexes Gene Set

sleep apnea, obstructive; sleep deprivation Gene Set

circadian sleep/wake cycle, rem sleep Gene Set

regulation of circadian sleep/wake cycle, sleep Gene Set

positive regulation of circadian sleep/wake cycle, sleep Gene Set

regulation of circadian sleep/wake cycle, rem sleep Gene Set

negative regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

circadian sleep/wake cycle, non-rem sleep Gene Set

regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

positive regulation of circadian sleep/wake cycle, rem sleep Gene Set

negative regulation of circadian sleep/wake cycle, sleep Gene Set

negative regulation of circadian sleep/wake cycle, rem sleep Gene Set

positive regulation of circadian sleep/wake cycle, non-rem sleep Gene Set

positive regulation of circadian sleep/wake cycle, REM sleep Gene Set

negative regulation of circadian sleep/wake cycle, REM sleep Gene Set

regulation of circadian sleep/wake cycle, sleep Gene Set

regulation of circadian sleep/wake cycle, non-REM sleep Gene Set

regulation of circadian sleep/wake cycle, REM sleep Gene Set

positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set

positive regulation of circadian sleep/wake cycle, sleep Gene Set

negative regulation of circadian sleep/wake cycle, sleep Gene Set

positive regulation of circadian sleep/wake cycle, REM sleep Gene Set

negative regulation of circadian sleep/wake cycle, REM sleep Gene Set

regulation of circadian sleep/wake cycle, sleep Gene Set

regulation of circadian sleep/wake cycle, non-REM sleep Gene Set

regulation of circadian sleep/wake cycle, REM sleep Gene Set

positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set

positive regulation of circadian sleep/wake cycle, sleep Gene Set

negative regulation of circadian sleep/wake cycle, sleep Gene Set

Sleep duration (short sleep) Gene Set

Sleep duration (long sleep) Gene Set

Brain Waves Gene Set

low amplitude p300 waves Gene Set

waves Gene Set

Brain Waves Gene Set

Emg Positive Sharp Waves Gene Set

Eeg With Focal Sharp Waves Gene Set

continuous performance task Gene Set

continuous Gene Set

Continuous Muscle Fiber Activity, Hereditary Gene Set

Continuous Leakage Of Urine Gene Set

Continuous Tremor Gene Set

Continuous Electrocardiogram Sinus Bradycardia (Finding) Gene Set

Continuous Electrocardiogram - Paroxysmal Supraventricular Tachycardia Gene Set

Response to lithium treatment in bipolar disorder (continuous phenotype) Gene Set

Insomnia complaints (continuous) Gene Set

Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) Gene Set

Neurocognitive impairment in HIV-1 infection (continuous) Gene Set

Bipolar disorder lithium response (continuous) or schizophrenia Gene Set

Number of stillbirths in continuous marriage Gene Set

Degraded stimulus continuous performance test score Gene Set

transition between fast and slow fiber Gene Set

transition between slow and fast fiber Gene Set

transition between fast and slow fiber Gene Set

transition between fast and slow fiber Gene Set

spike Gene Set

eeg with spike-wave complexes (>3.5 hz) Gene Set

eeg with spike-wave complexes Gene Set

abnormal spike wave discharge Gene Set

spike Gene Set

Eeg With Spike-Wave Complexes Gene Set

Eeg With Spike-Wave Complexes (2.5-3.5 Hz) Gene Set

Eeg With Spike-Wave Complexes (>3.5 Hz) Gene Set

abnormal spike wave discharge Gene Set