| Name |
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Central Sleep Apnea Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive sleep apnea during REM sleep (apnea hypopnea index) Gene SetFrom 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. |
Obstructive sleep apnea trait (apnea hypopnea index) Gene SetFrom 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. |
sleep apnea, obstructive; sleep deprivation Gene SetFrom 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. |
Obstructive sleep apnea (average oxygen saturation during sleep) Gene SetFrom 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. |
central sleep apnea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypercapnic respiratory failure; hypoventilation; sleep apnea, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Sleep Apnea, Central Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Central sleep apnea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
obstructive sleep apnea syndrome Gene SetFrom 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. |
Obstructive Sleep Apnea Hypopnea Syndrome Gene SetFrom 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. |
Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene SetFrom 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. |
Upper Airway Resistance Sleep Apnea Syndrome Gene SetFrom 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. |
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene SetFrom 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. |
Sleep Apnea, Obstructive Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea Syndromes from the curated CTD Gene-Disease Associations dataset. |
sleep apnea Gene SetFrom 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 SetFrom 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. |
cardiovascular diseases; sleep apnea, obstructive Gene SetFrom 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. |
hypertension; sleep apnea, obstructive; snoring Gene SetFrom 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. |
obesity; blood pressure, arterial; sleep apnea Gene SetFrom 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 SetFrom 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. |
sleep apnea, obstructive Gene SetFrom 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 SetFrom 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 SetFrom 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. |
cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene SetFrom 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. |
obesity; sleep apnea, obstructive Gene SetFrom 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. |
myocardial infarction; sleep apnea, obstructive Gene SetFrom 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 SetFrom 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 Gene SetFrom 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 apnea Gene SetFrom 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. |
Sleep Apnea, Obstructive Gene SetFrom 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 SetFrom 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 Gene SetFrom 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. |
Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene SetFrom 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. |
Obstructive Sleep Apnea Hypopnea Gene SetFrom 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. |
Severe Pediatric Obstructive Sleep Apnea Gene SetFrom 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. |
Sleep apnea Gene SetFrom 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 SetFrom 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 apnea Gene SetFrom 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 SetFrom 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. |
Mixed sleep apnea Gene SetFrom 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. |
Sleep apnea Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sleep apnea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Obstructive sleep apnea trait (average respiratory event duration) Gene SetFrom 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. |
Obstructive sleep apnea Gene SetFrom 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 SetFrom 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. |
central apnea Gene SetFrom HPO Gene-Disease Associations genes associated with the central apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Central Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
fatigue; sleep disorders; sleep initiation and maintenance disorders Gene SetFrom 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. |
circadian sleep/wake cycle, rem sleep Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene SetFrom 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. |
Congenital myasthenic syndrome with episodic apnea Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset. |
myasthenic syndrome, congenital, associated with episodic apnea Gene SetFrom OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset. |
central nervous system neoplasms; central nervous system tumors; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms; central nervous system tumors; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Apnea Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Apnea from the curated CTD Gene-Disease Associations dataset. |
apnea; opioid-related disorders; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea, post-succinylcholine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea, post-succinylcholine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
post-succinylcholine apnea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease post-succinylcholine apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term apnea in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
[125I]APNEA Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]APNEA ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
APNEA Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the APNEA ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
sudden episodic apnea Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden episodic apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
apnea Gene SetFrom HPO Gene-Disease Associations genes associated with the apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Apnea Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Apnea phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
apnea Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the apnea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
apnea, postanesthetic Gene SetFrom OMIM Gene-Disease Associations genes associated with the apnea, postanesthetic phenotype from the curated OMIM Gene-Disease Associations dataset. |
Sudden Episodic Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Episodic Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Induced Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Induced Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infantile Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infantile Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Apnea Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
apnea Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the apnea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Apnea Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Apnea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
APNEA Gene Setinteracting proteins for the APNEA drug from theDGIdb Drug Targets 2026 dataset. |
Advanced sleep phase syndrome, familial, 2 Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset. |
advanced sleep phase syndrome Gene SetFrom 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. |
delayed sleep phase syndrome Gene SetFrom 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. |
delayed sleep phase syndrome. Gene SetFrom 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; tourette syndrome Gene SetFrom 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. |
advanced sleep phase syndrome, familial, 1 Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the {delayed sleep phase syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
advanced sleep-phase syndrome, familial, 2 Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom 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. |
Insufficient Sleep Syndrome Gene SetFrom 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. |
Delayed sleep phase syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Advanced sleep phase syndrome 2 Gene SetFrom 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 SetFrom 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. |
Advanced sleep phase syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Advanced sleep phase syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Congenital central hypoventilation syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset. |
congenital central hypoventilation syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital central hypoventilation syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Hermansky-Pudlak syndrome 3, central region Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hermansky-Pudlak syndrome 3, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
central hypoventilation syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
central hypoventilation syndrome, congenital Gene SetFrom OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital phenotype from the curated OMIM Gene-Disease Associations dataset. |
Central Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital central hypoventilation syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital central hypoventilation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital central hypoventilation syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital central hypoventilation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Solitary median maxillary central incisor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Solitary median maxillary central incisor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central hypoventilation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypoventilation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sleep Deprivation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Deprivation from the curated CTD Gene-Disease Associations dataset. |
Sleep Initiation and Maintenance Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset. |
REM Sleep Behavior Disorder Gene SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders, Circadian Rhythm from the curated CTD Gene-Disease Associations dataset. |
Sleep Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders from the curated CTD Gene-Disease Associations dataset. |
Sleep Gene SetFrom 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 SetFrom 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 SetFrom 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. |
sleep disorder Gene SetFrom 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. |
bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders Gene SetFrom 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. |
sleep duration Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
sleep disorders; body mass Gene SetFrom 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. |
fatigue; sleep initiation and maintenance disorders Gene SetFrom 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. |
brain injuries; fatigue; sleep disorders Gene SetFrom 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. |
sleep initiation and maintenance disorders Gene SetFrom 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. |
hot flashes; osteoporosis, postmenopausal; sleep disorders Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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; schizophrenia; body mass Gene SetFrom 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. |
fatigue; neoplasms; sleep disorders Gene SetFrom 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. |
total energy intake and cytokine sleep factors Gene SetFrom 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 Gene SetFrom 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 SetFrom 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. |
alcoholism; sleep disorders Gene SetFrom 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. |
adhd; sleep Gene SetFrom 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. |
sleep Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the sleep disturbance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sleep-wake cycle disturbance Gene SetFrom 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 SetFrom 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. |
abnormal rapid eye movement (rem) sleep Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Initiation and Maintenance Disorders Gene SetFrom 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. |
REM Sleep Behavior Disorder Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom MPO Gene-Phenotype Associations gene mutations causing the fragmentation of sleep/wake states phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[respiratory rhythmicity in sleep] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [respiratory rhythmicity in sleep] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Non-24 Hour Sleep-Wake Disorder Gene SetFrom 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 SetFrom 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 SetFrom 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 Bruxism Gene SetFrom 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. |
Sleep-Disordered Breathing Gene SetFrom 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 And Maintenance Disorders Gene SetFrom 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. |
Sleep Initiation Dysfunction Gene SetFrom 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. |
Rem Sleep Behavior Disorder Gene SetFrom 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. |
Continuous Spike And Waves During Slow Sleep Gene SetFrom 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. |
Sleep-Related Respiratory Failure Gene SetFrom 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. |
Delayed Sleep Phase Gene SetFrom 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 SetFrom 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. |
Sudden Onset Of Sleep Gene SetFrom 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. |
Sleep Attack Gene SetFrom 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. |
Adjustment Sleep Disorder Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
decreased slow-wave sleep duration Gene SetFrom 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 SetFrom 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. |
abnormal sleep behavior Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal sleep behavior phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Sleep regulation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Sleep regulation pathway from the WikiPathways Pathways 2024 dataset. |
regulation of circadian sleep/wake cycle, wakefulness Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 disorder Gene SetFrom 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. |
REM sleep behavior disorder Gene SetFrom 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. |
Familial sleep-related hypermotor epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sleep-related hypermotor epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Continuous spike and waves during slow sleep Gene SetFrom 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. |
Sleep duration Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Night sleep phenotypes Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Sleep-related phenotypes Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central medullary reticular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
precentral gyrus, right, bank of the central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in precentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central nucleus, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, left, bank of the posterior central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, left, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central nucleus, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central gray substance of midbrain, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
precentral gyrus, left, bank of the central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in precentral gyrus, left, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central gray of the pons, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray of the pons, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central gray of the pons, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray of the pons, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central glial substance Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central glial substance relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, left, bank of the central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, left, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central gray substance of midbrain, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central medullary reticular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, right, bank of the central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, right, bank of the central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, right, bank of the posterior central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, right, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central part of MPO Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of MPO relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central amygdaloid nucleus, medial part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central amygdaloid nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central part of MD Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of MD relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central subpallium (classic basal ganglia) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central subpallium (classic basal ganglia) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Anterior hypothalamic nucleus, central part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pontine central gray Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pontine central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r4 liminal central gray Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r4 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central amygdalar nucleus, medial part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central lobule Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central lobule relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central lateral nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central lateral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central amygdalar nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central amygdalar nucleus, capsular part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, capsular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central part of VMH Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central part of VMH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Ventromedial hypothalamic nucleus, central part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventromedial hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior central nucleus raphe, lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior central nucleus raphe, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central amygdalar nucleus, lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central amygdalar nucleus, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central nucleus of the inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus of the inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Inferior colliculus, central nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Inferior colliculus, central nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central lateral nucleus of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central lateral nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior central nucleus raphe Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior central nucleus raphe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central medial nucleus of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central medial nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Parabrachial nucleus, lateral division, central lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Parabrachial nucleus, lateral division, central lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Mediodorsal nucleus of the thalamus, central part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Mediodorsal nucleus of the thalamus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r2 liminal central gray Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r2 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r3 liminal central gray Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r3 liminal central gray relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central layers of TG Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in central layers of TG relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
nucleus of the central acoustic tract Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the central acoustic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Central linear nucleus raphe Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Central linear nucleus raphe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
central portion of GPi Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central portion of GPi relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
central part of CEl Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central part of CEl relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
central nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
central nuclear group Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nuclear group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
medial subdivision of central nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in medial subdivision of central nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Hypothyroidism, central, and testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital central hypoventilation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central precocious puberty Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central core disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Single upper central incisor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
central element Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the central element cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear pore central transport channel Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
central element Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the central element cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
central vacuole Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the central vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Central Nervous System Agents Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Central Nervous System Agents from the curated CTD Gene-Chemical Interactions dataset. |
Cataract, Central Saccular, With Sutural Opacities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Central Saccular, With Sutural Opacities from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Central Core Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Central Core from the curated CTD Gene-Disease Associations dataset. |
Central Nervous System Infections Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Infections from the curated CTD Gene-Disease Associations dataset. |
Vasculitis, Central Nervous System Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vasculitis, Central Nervous System from the curated CTD Gene-Disease Associations dataset. |
Choroidal Dystrophy, Central Areolar 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset. |
Central Nervous System Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Diseases from the curated CTD Gene-Disease Associations dataset. |
Precocious Puberty, Central Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Precocious Puberty, Central from the curated CTD Gene-Disease Associations dataset. |
Central Nervous System Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Central Nervous System Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Choroidal dystrophy central areolar Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset. |
Hemangioma, Cavernous, Central Nervous System Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemangioma, Cavernous, Central Nervous System from the curated CTD Gene-Disease Associations dataset. |
Single upper central incisor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Single upper central incisor from the curated CTD Gene-Disease Associations dataset. |
Central Nervous System Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Central Nervous System in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
central nervous system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central nervous system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of central nervous system Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
central core myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central core myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
central nervous system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease central nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
central nervous system cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease central nervous system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
central nervous system lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
partial central choroid dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central core myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central core myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system origin vertigo Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system origin vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central epithelioid sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system hereditary degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system hereditary degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central pontine myelinolysis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system germinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system mesenchymal non-meningothelial tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of central nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
conventional central osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conventional central osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system primitive neuroectodermal neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system primitive neuroectodermal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central neurocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central neurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system melanocytic neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system melanocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system vasculitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central retinal artery occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central retinal vein occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hearing loss, central Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
loperamide disposition and central nervous system effects. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease loperamide disposition and central nervous system effects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus vasculitis, central nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus vasculitis, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; hemangioma, cavernous, central nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; hemangioma, cavernous, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; central nervous system vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; central nervous system vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus nephritis; lupus vasculitis, central nervous system; nephritis sle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus nephritis; lupus vasculitis, central nervous system; nephritis sle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggression, impulsivity, and central nervous system serotonergic responsivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggression, impulsivity, and central nervous system serotonergic responsivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central adiposity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central core disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central core disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system diseases; hiv infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system diseases; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central pulse pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central pulse pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system relapse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system relapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term central in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
central nervous system interneuron axonogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system interneuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system myelination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system vasculogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of central b cell tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of central b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system neuron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of central b cell tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of central b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
central tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system projection neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
axon ensheathment in central nervous system Gene SetFrom GO Biological Process Annotations 2015 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
central nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
central element Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the central element cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Central corneal thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
central nervous system disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease central nervous system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
central nervous system cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease central nervous system cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
neoplasm of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malignant neoplasm of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malignant neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
benign neoplasm of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the benign neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
central hypotonia Gene SetFrom HPO Gene-Disease Associations genes associated with the central hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant neoplasm of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central scotoma Gene SetFrom HPO Gene-Disease Associations genes associated with the central scotoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central hypothyroidism Gene SetFrom HPO Gene-Disease Associations genes associated with the central hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
benign neoplasm of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the benign neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dysplastic distal thumb phalanges with a central hole Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lipomas of the central neryous system Gene SetFrom HPO Gene-Disease Associations genes associated with the lipomas of the central neryous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central motor function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sudden central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
agenesis of central incisor Gene SetFrom HPO Gene-Disease Associations genes associated with the agenesis of central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widely-spaced maxillary central incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the widely-spaced maxillary central incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central opacification of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the central opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased central vision Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased central vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central diabetes insipidus Gene SetFrom HPO Gene-Disease Associations genes associated with the central diabetes insipidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
agenesis of mandibular central incisor Gene SetFrom HPO Gene-Disease Associations genes associated with the agenesis of mandibular central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central adrenal insufficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the central adrenal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macrodontia of permanent maxillary central incisor Gene SetFrom HPO Gene-Disease Associations genes associated with the macrodontia of permanent maxillary central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midline central nervous system lipomas Gene SetFrom HPO Gene-Disease Associations genes associated with the midline central nervous system lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene SetFrom HPO Gene-Disease Associations genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central hypoventilation Gene SetFrom HPO Gene-Disease Associations genes associated with the central hypoventilation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
central nervous system degeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the central nervous system degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large central visual field defect Gene SetFrom HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Central Serous Chorioretinopathy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Central Serous Chorioretinopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Central Nervous System Vascular Malformations Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Vascular Malformations phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Central Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Vasculitis, Central Nervous System Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Vasculitis, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Central Nervous System Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Central Nervous System Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Central Nervous System Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hemangioma, Cavernous, Central Nervous System Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hemangioma, Cavernous, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Central Nervous System Demyelinating Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Central Nervous System Demyelinating Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lupus Vasculitis, Central Nervous System Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lupus Vasculitis, Central Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
S-adenosylmethionine synthetase, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the S-adenosylmethionine synthetase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IA, central region, subdomain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IA, central region, subdomain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MDM2-binding protein, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MDM2-binding protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S4e, central region Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S4e, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Poly(A) polymerase, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Poly(A) polymerase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IIA, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IIA, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synaptonemal complex central element protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex central element protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IA, central Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, central protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Talin, central Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Talin, central protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acyl-CoA oxidase/dehydrogenase, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA oxidase/dehydrogenase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pro-opiomelanocortin/corticotropin, ACTH, central region Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pro-opiomelanocortin/corticotropin, ACTH, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TPX2 central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TPX2 central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thiamine pyrophosphate enzyme, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synaptonemal complex central element protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex central element protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FERM central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FERM central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sec16, central conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sec16, central conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Interleukin-12 beta, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Interleukin-12 beta, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Runx, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Runx, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein-arginine deiminase (PAD), central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-arginine deiminase (PAD), central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mur ligase, central Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mur ligase, central protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycoside hydrolase, family 65, central catalytic Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 65, central catalytic protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA ligase, ATP-dependent, central Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA ligase, ATP-dependent, central protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 8, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Developmental pluripotency-associated protein 2/4, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycoside hydrolase, family 38, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WASH complex subunit 7, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WASH complex subunit 7, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Elongation factor 1 beta central acidic region, eukaryote Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Elongation factor 1 beta central acidic region, eukaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dynamin central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dynamin central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycoside hydrolase, families 57/38, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, families 57/38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transcription elongation factor S-II, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription elongation factor S-II, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cactin, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cactin, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acetyl-CoA carboxylase, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-CoA carboxylase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell morphogenesis central region Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell morphogenesis central region protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal central pattern generator function Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal central tendon morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal central tendon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord central canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal central nervous system regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal central nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal central medial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal central medial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
precocious puberty, central, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the precocious puberty, central, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
single median maxillary central incisor Gene SetFrom OMIM Gene-Disease Associations genes associated with the single median maxillary central incisor phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic nerve hypoplasia and abnormalities of the central nervous system Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset. |
macular dystrophy with central cone involvement Gene SetFrom OMIM Gene-Disease Associations genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset. |
choriodal dystrophy, central areolar 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{efavirenz central nervous system toxicity, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {efavirenz central nervous system toxicity, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypothyroidism, central, and testicular enlargement Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypothyroidism, central, and testicular enlargement phenotype from the curated OMIM Gene-Disease Associations dataset. |
central core disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the central core disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
?precocious puberty, central, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?precocious puberty, central, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
central nervous system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue central nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
central nervous system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue central nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
central amygdaloid nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
central nervous system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
midbrain central gray Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue midbrain central gray in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
central medial thalamic nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue central medial thalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Central Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Neuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Depression (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Depression (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Central Nervous System Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Central Nervous System Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Serous Chorioretinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Core Myopathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Core Myopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ataxia With Central Nervous System Hypomyelinization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Demyelination Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Visual Impairment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Visual Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Central Serous Chorioretinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Precocious Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Retinal Vein Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Odontogenic Fibroma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Odontogenic Fibroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Metabolic Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Metabolic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metabolic Disorder, Central Nervous System, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Disorder, Central Nervous System, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Blindness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Central Precocious Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Solitary Median Maxillary Central Incisor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Solitary Median Maxillary Central Incisor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Of Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Angiitis Of The Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Angiitis Of The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Demyelinating Disease Of Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Demyelinating Disease Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Central Serous Chorioretinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Central Serous Chorioretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Central Hypoventilation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Leukaemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Leukaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Central Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Neurocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Neurocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Neoplasms, Primary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Neoplasms, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Auditory Processing Disorder, Central Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Auditory Processing Disorder, Central in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Large B-Cell Lymphoma Of Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Sensitization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Sensitization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Neuropathic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Central Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Candidiasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lupus Vasculitis, Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lupus Vasculitis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cavernous Angioma, Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cavernous Angioma, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Embryonal Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Embryonal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Embryonal Tumor, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Embryonal Tumor, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Germinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Germinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Choroidal Dystrophy, Central Areolar 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Areolar Choroidal Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Areolar Choroidal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Central Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Central Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Melanocytic Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Melanocytic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Retinal Artery Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vasculitis, Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vasculitis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Retinal Vein Occlusion - Juvenile Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion - Juvenile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysplastic Distal Thumb Phalanges With A Central Hole Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Choroidal Dystrophy, Central Areolar 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toxoplasmosis, Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toxoplasmosis, Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Centrifugal Cicatricial Alopecia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Centrifugal Cicatricial Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Hypogonadism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Core Disease, Autosomal Recessive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Core Disease, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Langerhans Cell Histiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Topographic Island Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Topographic Island in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Hemangioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Central Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Midline Central Nervous System Lipomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Midline Central Nervous System Lipomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Degeneration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Nervous System Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Corneal Thickness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Corneal Thickness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Hypotonia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Post-Stroke Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Post-Stroke Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Heterochromia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Heterochromia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widely-Spaced Maxillary Central Incisors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widely-Spaced Maxillary Central Incisors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Hypoventilation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Retinal Vessel Vascular Tortuosity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Retinal Vessel Vascular Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Y-Shaped Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Y-Shaped Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Opacification Of The Cornea Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Opacification Of The Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Central Somatosensory Evoked Potentials Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Somatosensory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Vertebral Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Vertebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eeg With Central Focal Spikes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Central Focal Spikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Cyanosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Cyanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Central Visual Field Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Core Regions In Muscle Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Core Regions In Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Central Sensory Function Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Sensory Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Central Motor Conduction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Central Motor Conduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Central Microtubular Pair Morphology Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy/Degeneration Affecting The Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
central nervous system development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelination Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2023 dataset. |
central tolerance induction to self antigen Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system projection neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system vasculogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
axonemal central apparatus assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
central nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
axon ensheathment in central nervous system Gene SetFrom GO Biological Process Annotations 2023 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal spinal cord central canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sperm axonemal central pair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sperm axonemal central pair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central medial nucleus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central medial nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central pattern generator function Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal diaphragm central tendon morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal diaphragm central tendon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal central nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased central memory CD4-positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased central memory CD8 positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased central memory CD4-positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD4-positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased central memory CD8 positive, alpha-beta T cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased central memory CD8 positive, alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - PBMC - L2 - CD4+ Central Memory T Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD4+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L2 - CD8+ Central Memory T Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L2 - CD8+ Central Memory T cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD4+ Central Memory T_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD4+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - PBMC - L3 - CD8+ Central Memory T_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L3 - CD8+ Central Memory T_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Liver - L2 - Vascual Central Venous Endothelial Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Liver - L2 - Vascual Central Venous Endothelial cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Central memory CD4+ T cell_Arthrosis_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Arthrosis_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T helper 1 cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T helper 1 cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peripheral blood_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peripheral blood_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the CD4+ central memory like T (Tcm-like) cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell precursor_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system stem cell_Fetal brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system stem cell_Fetal brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system-associated macrophage_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system-associated macrophage_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Brain_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Naïve or central memory T cell_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Naïve or central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central nervous system cell_Central nervous system_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central nervous system cell_Central nervous system_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Heart_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Intestine_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Lymph_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Lymph_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Lymphoid tissue_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Lymphoid tissue_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Ovary_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Ovary_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Peritoneal fluid_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Peritoneal fluid_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Spleen_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Spleen_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Spleen_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Spleen_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell precursor_Stomach_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell precursor_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory T cell_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory T cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD4+ T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD4+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory CD8+ T cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory CD8+ T cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Central memory regulatory T(cTreg) cell_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Central memory regulatory T(cTreg) cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
HDAC6 interactions in the central nervous system Gene SetFrom WikiPathways Pathways 2024 proteins participating in the HDAC6 interactions in the central nervous system pathway from the WikiPathways Pathways 2024 dataset. |
central nervous system development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system development biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelination Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelination biological process from the curated GO Biological Process Annotations 2025 dataset. |
central tolerance induction to self antigen Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central tolerance induction to self antigen biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system projection neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system projection neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron development biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system vasculogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system vasculogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
axonemal central apparatus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the axonemal central apparatus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
central nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the central nervous system myelin formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
axon ensheathment in central nervous system Gene SetFrom GO Biological Process Annotations 2025 genes participating in the axon ensheathment in central nervous system biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of central tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of central tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of central B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central precocious puberty Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central precocious puberty from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central nervous system cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central diabetes insipidus Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Central diabetes insipidus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of central nervous system in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system vasculitis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Central nervous system vasculitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of central nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central diabetes insipidus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central diabetes insipidus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central conducting lymphatic anomaly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central conducting lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central pontine myelinolysis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system neuroblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system vasculitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system vasculitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central retinal vein occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal vein occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system hematologic cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hematologic cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central retinal artery occlusion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central retinal artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial central choroid dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Solitary median maxillary central incisor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Solitary median maxillary central incisor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system melanocytic neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system melanocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary diffuse large B-cell lymphoma of the central nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary diffuse large B-cell lymphoma of the central nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system mesenchymal non-meningothelial tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central epithelioid sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system germinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system tumor with BCOR internal tandem duplication Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central neurocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central neurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system immature teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system immature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system origin vertigo Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system origin vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system mature teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system mature teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adult central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system fibrosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central precocious puberty 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central precocious puberty 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system rhabdomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system angiosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Central nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Central nervous system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Midbrain central gray Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Midbrain central gray in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central amygdaloid nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central amygdaloid nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central medial thalamic nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Central medial thalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Central element Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Central element cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Axonemal central apparatus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Axonemal central apparatus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore central transport channel Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear pore central transport channel cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Axonemal central apparatus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central apparatus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Axonemal central pair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Axonemal central pair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central element Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central element cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central vacuole Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central vacuole cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central cylinder Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central cylinder cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central region of growth cone Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Central region of growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Nuclear pore central transport channel Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Central hypotonia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Spongy degeneration of central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongy degeneration of central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal central motor function Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal central motor function phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central precocious puberty Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital central hypoventilation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Optic nerve hypoplasia and abnormalities of the central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central scotoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central scotoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked central congenital hypothyroidism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked central congenital hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skeletal dysplasia and progressive central nervous system degeneration Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central core disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central areolar choroidal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central areolar choroidal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atrophy/Degeneration affecting the central nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central corneal thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure and central corneal thickness (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure and central corneal thickness (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central retinal vein equivalent Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal vein equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central retinal arteriolar equivalent Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central retinal arteriolar equivalent phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic central serous retinopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central serous retinopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central serous retinopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (early onset)(pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (early onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (late onset)(pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (late onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric central nervous system tumors (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corpus callosum central volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corpus callosum central volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Primary central nervous system lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary central nervous system lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Central carbon metabolism in cancer Gene SetFrom KEGG Pathways 2026 proteins participating in the Central carbon metabolism in cancer pathway from the KEGG Pathways 2026 dataset. |
Lynch syndrome:Turcot syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marfan's syndrome:Marfan's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
IFAP syndrome with or without BRESHECK syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome I:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset. |
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset. |
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cornelia de lange syndrome; de lange syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatigue syndrome, chronic; fatigue syndrome; postviral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
restless legs syndrome; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; uveomeningoencephalitic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melas syndrome; merrf syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angelman syndrome; rett syndrome; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
metabolic syndrome ; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
digeorge syndrome; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
down syndrome; ehlers-danlos syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart-hand syndrome, holt-oram syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene SetFrom GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
digeorge syndrome/velocardiofacial syndrome complex-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ifap syndrome with or without bresheck syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Crouzon syndrome-acanthosis nigricans syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crouzon syndrome-acanthosis nigricans syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Crouzon syndrome-acanthosis nigricans syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Crouzon syndrome-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
Branchiootic syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branchiootic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bartter syndrome, type 3, with hypocalciuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom 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. |
Multiple synostoses syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sjögren-Larsson syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sjögren-Larsson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hennekam lymphangiectasia-lymphedema syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hennekam lymphangiectasia-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
UV-sensitive syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the UV-sensitive syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib-polydactyly syndrome, Majewski type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Char syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Char syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fragile X syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fragile X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Shwachman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Shwachman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Greig cephalopolysyndactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Greig cephalopolysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Melnick-Fraser syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Melnick-Fraser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marfan's syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Melnick-Needles syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Melnick-Needles syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Branchiootorenal syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branchiootorenal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PTEN hamartoma tumor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PTEN hamartoma tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lesch-Nyhan syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lesch-Nyhan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oculofaciocardiodental syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oculofaciocardiodental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Robinow Sorauf syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Robinow Sorauf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
17q2131 microdeletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 17q2131 microdeletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Desbuquois syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Desbuquois syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly/autism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly/autism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, type 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephrotic syndrome, type 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mohr-Tranebjaerg syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mohr-Tranebjaerg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Osteopenic nonfracture syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Osteopenic nonfracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Barakat syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Barakat syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Raine syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Raine syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digitorenocerebral syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Digitorenocerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ataxia-telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alport syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alstrom syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alstrom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinism-hyperammonemia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Joubert syndrome 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal multiple pterygium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MORM syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MORM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Upshaw-Schulman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Upshaw-Schulman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Martsolf syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Martsolf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Usher syndrome, type 1D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom 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. |
Usher syndrome, type 1J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chromosome 2q32-q33 deletion syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blepharophimosis-ptosis-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Borrone Di Rocco Crovato syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Borrone Di Rocco Crovato syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hurler syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hurler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angelman syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angelman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lig4 syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lig4 syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rubinstein-Taybi syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hajdu-Cheney syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hajdu-Cheney syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperferritinemia cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Temtamy preaxial brachydactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Temtamy preaxial brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial DNA depletion syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin E syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bannayan-Riley-Ruvalcaba syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bannayan-Riley-Ruvalcaba syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chudley-McCullough syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chudley-McCullough syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poretti-boltshauser syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poretti-boltshauser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frank Ter Haar syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frank Ter Haar syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Androgen resistance syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoparathyroidism retardation dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |