Obstructive Sleep Apnea Hypopnea Syndrome

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Results for "Obstructive Sleep Apnea Hypopnea Syndrome": 31 genes, 1001 gene sets

Name
RRIS Gene Respiratory rhythmicity in sleep
COPD14 Gene Chronic obstructive* pulmonary disease QTL 14*
COPD3 Gene Chronic obstructive* pulmonary disease QTL 3*
COPD2 Gene Chronic obstructive* pulmonary disease QTL 2*
COPD1 Gene Chronic obstructive* pulmonary disease QTL 1*
COPD6 Gene Chronic obstructive* pulmonary disease QTL 6*
COPD5 Gene Chronic obstructive* pulmonary disease QTL 5*
COPD4 Gene Chronic obstructive* pulmonary disease QTL 4*
COPD8 Gene Chronic obstructive* pulmonary disease QTL 8*
COPD17 Gene Chronic obstructive* pulmonary disease QTL 17*
COPD7 Gene Chronic obstructive* pulmonary disease QTL 7*
COPD9 Gene Chronic obstructive* pulmonary disease QTL 9*
COPD13 Gene Chronic obstructive* pulmonary disease QTL 13*
COPD12 Gene Chronic obstructive* pulmonary disease QTL 12*
COPD11 Gene Chronic obstructive* pulmonary disease QTL 11*
COPD10 Gene Chronic obstructive* pulmonary disease QTL 10*
COPD16 Gene Chronic obstructive* pulmonary disease QTL 16*
COPD15 Gene Chronic obstructive* pulmonary disease QTL 15*
COPD19 Gene Chronic obstructive* pulmonary disease QTL 19*
COPD18 Gene Chronic obstructive* pulmonary disease QTL 18*
COPD Gene Pulmonary disease, chronic obstructive, severe early-onset
COPD28 Gene Chronic obstructive* pulmonary disease QTL 28*
COPD29 Gene Chronic obstructive* pulmonary disease QTL 29*
COPD22 Gene Chronic obstructive* pulmonary disease QTL 22*
COPD23 Gene Chronic obstructive* pulmonary disease QTL 23*
COPD20 Gene Chronic obstructive* pulmonary disease QTL 20*
COPD21 Gene Chronic obstructive* pulmonary disease QTL 21*
COPD26 Gene Chronic obstructive* pulmonary disease QTL 26*
COPD27 Gene Chronic obstructive* pulmonary disease QTL 27*
COPD24 Gene Chronic obstructive* pulmonary disease QTL 24*
COPD25 Gene Chronic obstructive* pulmonary disease QTL 25*
Obstructive Sleep Apnea Hypopnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Sleep Apnea Hypopnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive sleep apnea during REM sleep (apnea hypopnea index) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea during REM sleep (apnea hypopnea index) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea trait (apnea hypopnea index) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea trait (apnea hypopnea index) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive Sleep Apnea Hypopnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Sleep Apnea Hypopnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
sleep apnea, obstructive; sleep deprivation Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea, obstructive; sleep deprivation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Obstructive sleep apnea (average oxygen saturation during sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea (average oxygen saturation during sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
obstructive sleep apnea syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease obstructive sleep apnea syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sleep Apnea, Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea, Obstructive from the curated CTD Gene-Disease Associations dataset.
hypertension; inflammation; obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; inflammation; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; sleep apnea, obstructive; snoring Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; sleep apnea, obstructive; snoring in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; sleep apnea, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstructive sleep apnea Gene Set From HPO Gene-Disease Associations genes associated with the obstructive sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sleep Apnea, Obstructive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Obstructive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Pediatric Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Pediatric Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive sleep apnea Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Obstructive sleep apnea in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive sleep apnea trait (average respiratory event duration) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea trait (average respiratory event duration) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obstructive sleep apnea (BMI adjusted) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obstructive sleep apnea (BMI adjusted) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Central Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Airway Resistance Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Resistance Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Apnea Gene Set From 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.
Hypopnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypopnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Apnea Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Apnea Syndromes from the curated CTD Gene-Disease Associations dataset.
central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obesity; blood pressure, arterial; sleep apnea Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercapnic respiratory failure; hypoventilation; sleep apnea, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep apnea Gene Set From HPO Gene-Disease Associations genes associated with the sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sleep Apnea Syndromes Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea, Central Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Apnea, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep apnea Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sleep apnea in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed sleep apnea Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep apnea Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sleep apnea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic Obstructive Asthma (With Obstructive Pulmonary Disease) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Obstructive Asthma (With Obstructive Pulmonary Disease) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive sleep apnea_Hepatic Tissue_GSE1873 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Obstructive sleep apnea_Hepatic Tissue_GSE1873 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
hypopnea Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hypopnea in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
hypopnea Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hypopnea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hypopnea Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hypopnea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fatigue; sleep disorders; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep disorders; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of circadian sleep/wake cycle, rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of circadian sleep/wake cycle, rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, non-rem sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, non-rem sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle, REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, non-REM sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, non-REM sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of circadian sleep/wake cycle, sleep Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of circadian sleep/wake cycle, sleep biological process from the curated GO Biological Process Annotations 2025 dataset.
Sleep duration (short sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (short sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (long sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (long sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Congenital myasthenic syndrome with episodic apnea Gene Set From 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 Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset.
Asthma-chronic obstructive pulmonary disease overlap syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma-chronic obstructive pulmonary disease overlap syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Apnea Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
central apnea Gene Set From 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.
apnea Gene Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the apnea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
apnea, postanesthetic Gene Set From OMIM Gene-Disease Associations genes associated with the apnea, postanesthetic phenotype from the curated OMIM Gene-Disease Associations dataset.
Sudden Episodic Apnea Gene Set From 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 Set From 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.
Central Apnea Gene Set From 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.
Infantile Apnea Gene Set From 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 Set From 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 Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the apnea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Apnea Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Apnea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
APNEA Gene Set From DGIdb Drug Targets 2026 interacting proteins for the APNEA drug from theDGIdb Drug Targets 2026 dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
advanced sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
delayed sleep phase syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed sleep phase syndrome. Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
advanced sleep phase syndrome, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{delayed sleep phase syndrome, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {delayed sleep phase syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep-phase syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Advanced Sleep Phase Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep Phase Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Sleep Phase Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insufficient Sleep Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insufficient Sleep Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Delayed sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Advanced sleep phase syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Advanced sleep phase syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-hypotonia-spasticity-sleep disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Advanced sleep phase syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Advanced sleep phase syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From 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.
Pulmonary Disease, Chronic Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset.
Jaundice, Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Obstructive from the curated CTD Gene-Disease Associations dataset.
Lung Diseases, Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lung Diseases, Obstructive from the curated CTD Gene-Disease Associations dataset.
Pulmonary Disease, Chronic Obstructive Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
obstructive lung disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease obstructive lung disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
obstructive lung disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease obstructive lung disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
chronic obstructive pulmonary disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease chronic obstructive pulmonary disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
obstructive hydrocephalus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obstructive hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obstructive jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obstructive jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obstructive lung disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obstructive lung disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic obstructive pulmonary disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic obstructive pulmonary disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, pulmonary; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occupational diseases; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease occupational diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive airways disease. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive airways disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; asthma; thromboembolism, venous; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nephropathy, congenital obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease nephropathy, congenital obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
copd ; chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease copd ; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial hyperreactivity; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial hyperreactivity; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; lung diseases, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; lung diseases, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; eczema allergic; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases, obstructive; scleroderma, systemic; systemic scleroderma Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases, obstructive; scleroderma, systemic; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
emphysema; pulmonary disease, chronic obstructive; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease emphysema; pulmonary disease, chronic obstructive; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchiectasis; bronchitis; bronchitis unspecified; emphysema; lung diseases, obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchiectasis; bronchitis; bronchitis unspecified; emphysema; lung diseases, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; dermatitis, atopic; chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; dermatitis, atopic; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; kidney failure, acute; postoperative complications; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; kidney failure, acute; postoperative complications; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
emphysema; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease emphysema; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthenia; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease asthenia; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstructive pulmonary disease and disseminated bronchiectasis Gene Set From GAD Gene-Disease Associations genes associated with the disease obstructive pulmonary disease and disseminated bronchiectasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; chronic obstructive pulmonary disease Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease ; asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease ; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cough; dyspnea; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease cough; dyspnea; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease/copd; emphysema Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstructive Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term obstructive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
COPD - Chronic obstructive pulmonary disease_Lung Tissue_GSE1650 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Lung Tissue_GSE1650 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
COPD - Chronic obstructive pulmonary disease_Bronchial epithelium_GSE3320 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Bronchial epithelium_GSE3320 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Asthma or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Body mass in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic obstructive pulmonary disease (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Non-obstructive azoospermia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Non-obstructive azoospermia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic obstructive pulmonary disease (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic obstructive pulmonary disease-related biomarkers Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic obstructive pulmonary disease-related biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
obstructive lung disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease obstructive lung disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
chronic obstructive pulmonary disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease chronic obstructive pulmonary disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
non-obstructive azoospermia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the non-obstructive azoospermia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
obstructive lung disease Gene Set From GWASdb SNP-Phenotype Associations genes associated with the obstructive lung disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
chronic obstructive pulmonary disease Gene Set From GWASdb SNP-Phenotype Associations genes associated with the chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
chronic obstructive pulmonary disease Gene Set From HPO Gene-Disease Associations genes associated with the chronic obstructive pulmonary disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
obstructive lung disease Gene Set From HPO Gene-Disease Associations genes associated with the obstructive lung disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Pulmonary Disease, Chronic Obstructive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Disease, Chronic Obstructive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lung Diseases, Obstructive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lung Diseases, Obstructive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
non-obstructive hydrocephaly Gene Set From MPO Gene-Phenotype Associations gene mutations causing the non-obstructive hydrocephaly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
obstructive hydrocephaly Gene Set From MPO Gene-Phenotype Associations gene mutations causing the obstructive hydrocephaly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{pulmonary disease, chronic obstructive, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary disease, chronic obstructive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary disease, chronic obstructive, severe early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
Chronic Obstructive Airway Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Obstructive Airway Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Obstructive Azoospermia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Obstructive Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Obstructive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Obstructive Reflux-Associated Chronic Pyelonephritis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Obstructive Reflux-Associated Chronic Pyelonephritis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Azoospermia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Chronic Obstructive Pulmonary Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Chronic Obstructive Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Obstructive Azoospermia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Nephropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Ureterocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Ureterocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Chronic Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Obstructive Azoospermia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Ventilatory Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Obstructive Pulmonary Disease Exacerbation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Obstructive Pulmonary Disease Exacerbation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Moderate Chronic Obstructive Pulmonary Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Moderate Chronic Obstructive Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Obstructive Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Obstructive Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Asymmetric Septal Hypertrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Asymmetric Septal Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Sialadenitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Sialadenitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Exacerbation Of Chronic Obstructive Bronchitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Exacerbation Of Chronic Obstructive Bronchitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Emphysema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Obstructive Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Obstructive Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Exacerbation Of Chronic Obstructive Airways Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Exacerbation Of Chronic Obstructive Airways Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
non-obstructive hydrocephaly Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the non-obstructive hydrocephaly phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
obstructive hydrocephaly Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the obstructive hydrocephaly phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Obstructive lung disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Obstructive lung disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic obstructive pulmonary disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Chronic obstructive pulmonary disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic obstructive pulmonary disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic obstructive pulmonary disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive lung disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive lung disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive nephropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive hydrocephalus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Obstructive azoospermia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obstructive azoospermia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-obstructive azoospermia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-obstructive azoospermia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic bronchitis and chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic bronchitis and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic bronchitis in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic bronchitis in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (change over time) in gastrointestinal cancer or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in gastrointestinal cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (change over time) in cancer or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (change over time) in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (change over time) in lung cancer or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (change over time) in lung cancer or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Current cigarettes per day in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Current cigarettes per day in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease or resting heart rate (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or resting heart rate (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pulmonary artery enlargement and chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary artery enlargement and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pulmonary artery enlargement in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary artery enlargement in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease (moderate to severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease (moderate to severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Airway responsiveness in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Airway responsiveness in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma or chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma or chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease-related biomarkers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease-related biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cotinine levels in smokers with chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cotinine levels in smokers with chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Smoking cessation in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Smoking cessation in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exhaled carbon monoxide levels in smokers with chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exhaled carbon monoxide levels in smokers with chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early chronic obstructive pulmonary disease in never smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early chronic obstructive pulmonary disease in never smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-obstructive azoospermia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-obstructive azoospermia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age at smoking initiation in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at smoking initiation in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lifetime average cigarettes per day in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lifetime average cigarettes per day in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (inherited effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Change in quality of life in response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Change in quality of life in response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease x ever smoker interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease x ever smoker interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease in ever smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease in ever smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease x current smoker interaction (2df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease x current smoker interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease x ever smoker interaction (1df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease x ever smoker interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease in non-current smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease in non-current smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease x current smoker interaction (main effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease x current smoker interaction (main effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease x current smoker interaction (1df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease x current smoker interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease in current smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease in current smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep Deprivation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Deprivation from the curated CTD Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.
REM Sleep Behavior Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.
Sleep Bruxism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Bruxism from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders, Circadian Rhythm from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders from the curated CTD Gene-Disease Associations dataset.
Sleep Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Sleep in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sleep disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep duration Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep duration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep deprivation Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep deprivation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders, circadian rhythm Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders, circadian rhythm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; fatigue; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; fatigue; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hot flashes; osteoporosis, postmenopausal; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hot flashes; osteoporosis, postmenopausal; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep-disordered breathing Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep-disordered breathing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; schizophrenia; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; neoplasms; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; neoplasms; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
total energy intake and cytokine sleep factors Gene Set From GAD Gene-Disease Associations genes associated with the disease total energy intake and cytokine sleep factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd; sleep Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd; sleep in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term sleep in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle process Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle process biological process from the curated GO Biological Process Annotations 2015 dataset.
sleep Gene Set From GO Biological Process Annotations 2015 genes participating in the sleep biological process from the curated GO Biological Process Annotations 2015 dataset.
circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2015 genes participating in the circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
Sleep time Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep depth Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep depth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep quality Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep quality phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep-related phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sleep disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sleep disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sleep-wake cycle disturbance Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sleep-wake cycle disturbance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sleep disturbance Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sleep disturbance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sleep-wake cycle disturbance Gene Set From HPO Gene-Disease Associations genes associated with the sleep-wake cycle disturbance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sleep disturbance Gene Set From HPO Gene-Disease Associations genes associated with the sleep disturbance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal rapid eye movement (rem) sleep Gene Set From HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Circadian Rhythm phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Deprivation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Deprivation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Arousal Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Arousal Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Initiation and Maintenance Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
REM Sleep Behavior Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the REM Sleep Behavior Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Bruxism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Bruxism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep, REM Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep, REM phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Stages Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Stages phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders, Intrinsic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Intrinsic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal paradoxical sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sleep behavior Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sleep behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal frequency of paradoxical sleep Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal frequency of paradoxical sleep phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fragmentation of sleep/wake states Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fragmentation of sleep/wake states phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[respiratory rhythmicity in sleep] Gene Set From OMIM Gene-Disease Associations genes associated with the [respiratory rhythmicity in sleep] phenotype from the curated OMIM Gene-Disease Associations dataset.
Non-24 Hour Sleep-Wake Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-24 Hour Sleep-Wake Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonorganic Sleep Wake Cycle Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonorganic Sleep Wake Cycle Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Shift-Work Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Shift-Work Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Bruxism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Bruxism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Disordered Breathing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Disordered Breathing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation And Maintenance Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation And Maintenance Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rem Sleep Behavior Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rem Sleep Behavior Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Continuous Spike And Waves During Slow Sleep Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Continuous Spike And Waves During Slow Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Related Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Related Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Sleep Phase Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Onset Of Sleep Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Onset Of Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Attack Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Attack in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adjustment Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adjustment Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Environmental Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Environmental Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limit-Setting Sleep Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limit-Setting Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Disorders, Extrinsic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Disorders, Extrinsic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep-Related Painful Erections Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep-Related Painful Erections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duration Of Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duration Of Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Disturbances Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Disturbances in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
[D]Sleep Disturbances (& [Hypersomnia] Or [Insomnia]) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype [D]Sleep Disturbances (& [Hypersomnia] Or [Insomnia]) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Wake Cycle Disturbance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Wake Cycle Disturbance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Deprivation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Deprivation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rem Sleep Deprivation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rem Sleep Deprivation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Related Neurogenic Tachypnea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Related Neurogenic Tachypnea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Onset Latency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Onset Latency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Advanced Sleep Phase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Sleep Phase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Rapid Eye Movement Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Rapid Eye Movement Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Sleep Phase Disorder, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Sleep Phase Disorder, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fragmented Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fragmented Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Restless Sleep Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restless Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Onset Insomnia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Onset Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Non-Organic Sleep Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Non-Organic Sleep Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep Fragmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep Fragmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sleep-Wake Inversion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sleep-Wake Inversion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep duration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep duration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal circadian sleep/wake cycle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circadian sleep/wake cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal paradoxical sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fragmentation of sleep/wake states Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fragmentation of sleep/wake states phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep behavior Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep behavior phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased frequency of paradoxical sleep Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased frequency of paradoxical sleep phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased slow-wave sleep duration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased slow-wave sleep duration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal slow-wave sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal slow-wave sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep behavior Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal sleep behavior phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Sleep regulation Gene Set From WikiPathways Pathways 2024 proteins participating in the Sleep regulation pathway from the WikiPathways Pathways 2024 dataset.
regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of circadian sleep/wake cycle, wakefulness Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of circadian sleep/wake cycle, wakefulness biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of circadian sleep/wake cycle Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of circadian sleep/wake cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
Sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sleep disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
REM sleep behavior disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease REM sleep behavior disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial sleep-related hypermotor epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sleep-related hypermotor epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Continuous spike and waves during slow sleep Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Continuous spike and waves during slow sleep phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep traits (multi-trait analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep traits (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (oversleepers vs undersleepers) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (oversleepers vs undersleepers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Night sleep phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Night sleep phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Daytime sleep phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Daytime sleep phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x short total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x short total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (> 10 hours) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (> 10 hours) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1/2-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1/2-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep start time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep start time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1/3-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1/3-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep end time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep end time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (1-day periodicity) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (1-day periodicity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep activity levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep activity levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep-related phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep time Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep time phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep quality Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep quality phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertension risk in short sleep duration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep latency Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep latency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depressive symptom (sleep problems) (binary trait) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depressive symptom (sleep problems) (binary trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep (number of episodes) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep (number of episodes) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Lynch syndrome:Turcot syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
Branchiootic syndrome 3 Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 3 Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib-polydactyly syndrome, Majewski type Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Char syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fragile X syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fragile X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Shwachman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Shwachman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Greig cephalopolysyndactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Greig cephalopolysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Fraser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Fraser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Needles syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Needles syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Branchiootorenal syndrome 2 Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Lesch-Nyhan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculofaciocardiodental syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculofaciocardiodental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow Sorauf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow Sorauf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
17q2131 microdeletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 17q2131 microdeletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Desbuquois syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Desbuquois syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly/autism syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopenic nonfracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Barakat syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Barakat syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Raine syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Raine syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digitorenocerebral syndrome Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alstrom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alstrom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinism-hyperammonemia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 17 Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MORM syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MORM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Upshaw-Schulman syndrome Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Martsolf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Martsolf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1D Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1J Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hurler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angelman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angelman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lig4 syndrome Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hajdu-Cheney syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperferritinemia cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temtamy preaxial brachydactyly syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Chudley-McCullough syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poretti-boltshauser syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holt-Oram syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holt-Oram syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Young Simpson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Young Simpson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frasier syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frasier syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meier-Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meier-Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pili torti-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pili torti-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carpenter syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane-radial ray syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane-radial ray syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
22q133 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 22q133 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa-corneal clouding-oligophrenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TNF receptor-associated periodic fever syndrome (TRAPS) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Waardenburg syndrome type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Steel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Steel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 1q43-q44 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Roberts-SC phocomelia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Roberts-SC phocomelia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bloom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bloom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
McLeod neuroacanthocytosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the McLeod neuroacanthocytosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nicolaides-Baraitser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nicolaides-Baraitser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nager syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nager syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chédiak-Higashi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chédiak-Higashi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kindler's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kindler's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnevale syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnevale syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kenny syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kenny syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rienhoff syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rienhoff syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weaver syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weaver syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia/short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Siderius X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kohlschutter's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kohlschutter's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with marfanoid habitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebro-oculo-facio-skeletal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebro-oculo-facio-skeletal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis-lymphedema-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LEOPARD syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LEOPARD syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Treacher collins syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Treacher collins syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wiskott-Aldrich syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wiskott-Aldrich syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyper-IgE syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyper-IgE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tourette Syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tourette Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, macrosomia, facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gamstorp-Wohlfart syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gamstorp-Wohlfart syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyaline fibromatosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyaline fibromatosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weill-Marchesani-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weill-Marchesani-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Netherton syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Netherton syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome, type 4b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Feingold syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Feingold syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Waardenburg syndrome type 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Richieri Costa Pereira syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Richieri Costa Pereira syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune lymphoproliferative syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wilson-Turner X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Costello syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Costello syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ochoa syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ochoa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bruck syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bruck syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Achalasia-alacrima syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Achalasia-alacrima syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cryptophthalmos syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cryptophthalmos syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nijmegen breakage syndrome-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ovarian hyperstimulation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ovarian hyperstimulation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Otofaciocervical syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Otofaciocervical syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kaufman oculocerebrofacial syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kaufman oculocerebrofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Branchiooculofacial syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiooculofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Karak syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Karak syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky Pudlak syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky Pudlak syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tarsal carpal coalition syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tarsal carpal coalition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jankovic Rivera syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jankovic Rivera syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nakajo syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nakajo syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome Xq28 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi-Bickel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi-Bickel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
short QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Smith-Lemli-Opitz syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Smith-Lemli-Opitz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome progeroid type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Larsen syndrome, dominant type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, musculocontractural type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temtamy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Temtamy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Birk Barel mental retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alport syndrome, X-linked recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenomatous polyposis coli:Gardner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adenomatous polyposis coli:Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leprechaunism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leprechaunism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Simpson-Golabi-Behmel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Simpson-Golabi-Behmel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
XFE progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the XFE progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dysequilibrium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dysequilibrium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atypical hemolytic-uremic syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atypical hemolytic-uremic syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Johanson-Blizzard syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Johanson-Blizzard syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GRACILE syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GRACILE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked lymphoproliferative syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kowarski syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kowarski syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ADULT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ADULT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel-Gruber syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel-Gruber syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked lymphoproliferative syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutrophil immunodeficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutrophil immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coffin-Lowry syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coffin-Lowry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, hydroxylysine-deficient Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, hydroxylysine-deficient phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pierson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pierson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pfeiffer syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pfeiffer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tricho-dento-osseous syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tricho-dento-osseous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mowat-Wilson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mowat-Wilson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jensen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jensen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Werner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Werner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aarskog syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aarskog syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enamel-renal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enamel-renal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Popliteal pterygium syndrome lethal type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Keutel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Keutel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Segawa syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Segawa syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple pterygium syndrome Escobar type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins-like syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins-like syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Klippel-Feil syndrome 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stiff skin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stiff skin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lenz microphthalmia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lenz microphthalmia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall/Stickler syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall/Stickler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schwartz Jampel syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Grebe syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Grebe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Saethre-Chotzen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Saethre-Chotzen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Floating-Harbor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Floating-Harbor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osler hemorrhagic telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osler hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wieacker syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wieacker syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kabuki make-up syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kabuki make-up syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cohen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cohen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oligodontia-colorectal cancer syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oligodontia-colorectal cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Filippi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Filippi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primrose syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primrose syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall-Smith syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall-Smith syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brittle cornea syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brittle cornea syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rotor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rotor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oral-facial-digital syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oral-facial-digital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrocallosal syndrome, Schinzel type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gray platelet syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gray platelet syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mast syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mast syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amish infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meacham syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meacham syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stormorken syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stormorken syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Opitz-Frias syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Opitz-Frias syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardio-facio-cutaneous syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardio-facio-cutaneous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Yunis Varon syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Yunis Varon syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cowden syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cowden syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mulibrey nanism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mulibrey nanism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ohdo syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ohdo syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Townes-Brocks-branchiootorenal-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Townes-Brocks-branchiootorenal-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SeSAME syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SeSAME syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Odontotrichomelic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Odontotrichomelic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome, type 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lowe syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lowe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, type 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, musculocontractural type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van Maldergem syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofaciodigital syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofaciodigital syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distichiasis-lymphedema syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distichiasis-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Townes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Townes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neu-Laxova syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neu-Laxova syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Winchester syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Winchester syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Unverricht-Lundborg syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Unverricht-Lundborg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Verheij syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Verheij syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rapp-Hodgkin ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Allan-Herndon-Dudley syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Allan-Herndon-Dudley syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arterial tortuosity syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arterial tortuosity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Papillon-Lefèvre syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Papillon-Lefèvre syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brown-vialetto-van laere syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brown-vialetto-van laere syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peters plus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peters plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulnar-mammary syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulnar-mammary syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-dependent diabetes mellitus secretory diarrhea syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-dependent diabetes mellitus secretory diarrhea syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zunich neuroectodermal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beckwith-Wiedemann syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beckwith-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van Maldergem Wetzburger Verloes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem Wetzburger Verloes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sotos' syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sotos' syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyggve-Melchior-Clausen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dyggve-Melchior-Clausen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Baraitser-Winter Syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Baraitser-Winter Syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Three M syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Three M syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Howel-Evans syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Howel-Evans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhabdoid tumor predisposition syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tatton-Brown-rahman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tatton-Brown-rahman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
COACH syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the COACH syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enhanced s-cone syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enhanced s-cone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hydrocephalus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acquired long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van der Woude syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van der Woude syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sudden infant death syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dursun syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dursun syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carpenter syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Li-Fraumeni syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Li-Fraumeni syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Haim-Munk syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Haim-Munk syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knobloch syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knobloch syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carbohydrate-deficient glycoprotein syndrome type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carbohydrate-deficient glycoprotein syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoplastic enamel-onycholysis-hypohidrosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoplastic enamel-onycholysis-hypohidrosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jarcho-Levin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jarcho-Levin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive Dejerine-Sottas syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive Dejerine-Sottas syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kabuki syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kabuki syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hay-Wells syndrome of ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hay-Wells syndrome of ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reynolds syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reynolds syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glut1 deficiency syndrome 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 12/15, digenic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 12/15, digenic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Serkal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Serkal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marinesco-Sjögren syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marinesco-Sjögren syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neu-laxova syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neu-laxova syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Urofacial syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Urofacial syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gordon's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gordon's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arts syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
McKusick Kaufman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the McKusick Kaufman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rubinstein-Taybi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
FG syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the FG syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglandular autoimmune syndrome, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglandular autoimmune syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
EEM syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the EEM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiofaciocutaneous syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiofaciocutaneous syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TARP syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TARP syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Drash syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Drash syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pallister-Hall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pallister-Hall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Radial aplasia-thrombocytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Griscelli syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Griscelli syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Griscelli syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Griscelli syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Caudal regression syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Caudal regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Catel Manzke syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Catel Manzke syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trichohepatoenteric syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trichohepatoenteric syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cockayne syndrome type A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cockayne syndrome type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

RRIS Gene

COPD14 Gene

COPD3 Gene

COPD2 Gene

COPD1 Gene

COPD6 Gene

COPD5 Gene

COPD4 Gene

COPD8 Gene

COPD17 Gene

COPD7 Gene

COPD9 Gene

COPD13 Gene

COPD12 Gene

COPD11 Gene

COPD10 Gene

COPD16 Gene

COPD15 Gene

COPD19 Gene

COPD18 Gene

COPD Gene

COPD28 Gene

COPD29 Gene

COPD22 Gene

COPD23 Gene

COPD20 Gene

COPD21 Gene

COPD26 Gene

COPD27 Gene

COPD24 Gene

COPD25 Gene

Obstructive Sleep Apnea Hypopnea Syndrome Gene Set

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

Obstructive sleep apnea trait (apnea hypopnea index) Gene Set

Obstructive Sleep Apnea Hypopnea Gene Set

sleep apnea, obstructive; sleep deprivation Gene Set

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

obstructive sleep apnea syndrome Gene Set

Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene Set

AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene Set

Sleep Apnea, Obstructive Gene Set

hypertension; inflammation; obesity; sleep apnea, obstructive Gene Set

cardiovascular diseases; sleep apnea, obstructive Gene Set

hypertension; sleep apnea, obstructive; snoring Gene Set

sleep apnea, obstructive Gene Set

cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene Set

obesity; sleep apnea, obstructive Gene Set

myocardial infarction; sleep apnea, obstructive Gene Set

obstructive sleep apnea Gene Set

Sleep Apnea, Obstructive Gene Set

Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene Set

Severe Pediatric Obstructive Sleep Apnea Gene Set

Obstructive sleep apnea Gene Set

Obstructive sleep apnea Gene Set

Obstructive sleep apnea trait (average respiratory event duration) Gene Set

Obstructive sleep apnea Gene Set

Obstructive sleep apnea (BMI adjusted) Gene Set

Central Sleep Apnea Syndrome Gene Set

Upper Airway Resistance Sleep Apnea Syndrome Gene Set

Obstructive Apnea Gene Set

Hypopnea Syndrome Gene Set

Sleep Apnea Syndromes Gene Set

central sleep apnea Gene Set

sleep apnea Gene Set

obesity; blood pressure, arterial; sleep apnea Gene Set

memory disorders; sleep apnea syndromes Gene Set

sleep apnea syndromes Gene Set

sleep apnea Gene Set

hypercapnic respiratory failure; hypoventilation; sleep apnea, central Gene Set

cardiovascular diseases; sleep apnea syndromes Gene Set

sleep apnea Gene Set

Sleep Apnea Syndromes Gene Set

Sleep Apnea, Central Gene Set

Sleep Apnea Gene Set

Sleep apnea Gene Set

Sleep apnea Gene Set

Central sleep apnea Gene Set

Mixed sleep apnea Gene Set

Sleep apnea Gene Set

[¹²⁵I]APNEA Gene Set