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Episodic pain syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
episodic pain syndrome, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Episodic pain syndrome, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
episodic pain syndrome, familial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic pain syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial episodic pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial episodic pain syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial episodic pain syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial episodic pain syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial episodic pain syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial episodic pain syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial episodic pain syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic pain syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic pain syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
episodic abdominal pain Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic abdominal pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Episodic Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic kinesigenic dyskinesia and familial infantile convulsions Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia and familial infantile convulsions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
pain, postoperative; shoulder pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; shoulder pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain; shoulder pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain; shoulder pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; acute disease; low back pain; pain; sciatica Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; acute disease; low back pain; pain; sciatica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diarrhea; familial mediterranean fever; pain; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital myasthenic syndrome with episodic apnea Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset. |
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene SetFrom OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic ataxia/myokymia syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia/myokymia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
myasthenic syndrome, congenital, associated with episodic apnea Gene SetFrom OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset. |
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset. |
amyloidosis, familial; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; amyloidosis, familial; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple familial trichoepithelioma and familial cylindromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis, familial; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hemiplegic migraine and benign familial infantile convulsions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
patellofemoral pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease patellofemoral pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
myofascial pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myofascial pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
complex regional pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complex regional pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune diseases; pelvic pain; prostatitis; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; pelvic pain; prostatitis; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain; rett syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal pain; irritable bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal pain; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myofascial pain syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease myofascial pain syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Complex Regional Pain Syndrome I, Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complex Regional Pain Syndrome I, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Prostatitis With Chronic Pelvic Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Prostatitis With Chronic Pelvic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Post-Thoracotomy Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Post-Thoracotomy Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Calcineurin Inhibitor Induced Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Calcineurin Inhibitor Induced Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Total Body Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Total Body Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abdominal Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Pelvic Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Pelvic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Vertebrogenic Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vertebrogenic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Complex regional pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex regional pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofascial pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofascial pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Patellofemoral pain syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Patellofemoral pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital insensitivity to pain-hypohidrosis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital insensitivity to pain-hypohidrosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic ataxia, type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Choreoathetosis/spasticity, episodic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Choreoathetosis/spasticity, episodic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic ataxia type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic ataxia type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic Kinesigenic Dyskinesia 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Kinesigenic Dyskinesia 1 from the curated CTD Gene-Disease Associations dataset. |
Episodic ataxia with nystagmus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic ataxia with nystagmus from the curated CTD Gene-Disease Associations dataset. |
Episodic Muscle Weakness, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Choreoathetosis/Spasticity, Episodic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis/Spasticity, Episodic from the curated CTD Gene-Disease Associations dataset. |
Episodic Ataxia, Type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 3 from the curated CTD Gene-Disease Associations dataset. |
Episodic Ataxia, Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 1 from the curated CTD Gene-Disease Associations dataset. |
Episodic Ataxia, Type 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 7 from the curated CTD Gene-Disease Associations dataset. |
Episodic Ataxia, Type 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 5 from the curated CTD Gene-Disease Associations dataset. |
Episodic Ataxia, Type 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Ataxia, Type 6 from the curated CTD Gene-Disease Associations dataset. |
Episodic Kinesigenic Dyskinesia 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Kinesigenic Dyskinesia 2 from the curated CTD Gene-Disease Associations dataset. |
episodic ataxia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease episodic ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
episodic ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
episodic ataxia type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease episodic ataxia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
episodic memory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease episodic memory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
episodic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term episodic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
episodic tachypnea Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic tachypnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic ataxia Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic flaccid weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic flaccid weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic ketoacidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic ketoacidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic hyperhidrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic hyperhidrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sudden episodic apnea Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden episodic apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic vomiting Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic vomiting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic upper airway obstruction Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic peripheral neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intrahepatic cholestasis with episodic jaundice Gene SetFrom HPO Gene-Disease Associations genes associated with the intrahepatic cholestasis with episodic jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic fever Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic fever phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic quadriplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic metabolic acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic metabolic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic hemiplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic hemiplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic ammonia intoxication Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic ammonia intoxication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic hemolytic anemia Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic ataxia, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic ataxia, type 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic ataxia, type 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic ataxia, type 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic ataxia, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic kinesigenic dyskinesia 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic kinesigenic dyskinesia 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic kinesigenic dyskinesia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic kinesigenic dyskinesia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic muscle weakness, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
Episodic Kinesigenic Dyskinesia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Kinesigenic Dyskinesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Episodic Apnea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Episodic Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Ataxia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Quadriplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Generalized Hypotonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Generalized Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intrahepatic Cholestasis With Episodic Jaundice Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholestasis With Episodic Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Cluster Headache Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Cluster Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Tension-Type Headache Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Tension-Type Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Paroxysmal Anxiety Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Episodic Paroxysmal Anxiety in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Laryngospasm, Severe Neonatal Episodic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Laryngospasm, Severe Neonatal Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Choreoathetosis/Spasticity, Episodic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Choreoathetosis/Spasticity, Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Episodic Hemolytic Anemia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Vomiting Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Vomiting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Metabolic Acidosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Metabolic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Tachypnea Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Tachypnea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Ketoacidosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ketoacidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Respiratory Distress Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Respiratory Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hyperhidrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hyperhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Ammonia Intoxication Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ammonia Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hemiplegia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hemiplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Flaccid Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Flaccid Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hypokalemia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypokalemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Memory, Episodic Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory, Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Upper Airway Obstruction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hypoventilation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypoventilation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Ataxia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Defective SLC1A3 causes episodic ataxia 6 (EA6) Gene Setproteins participating in the Defective SLC1A3 causes episodic ataxia 6 (EA6) pathway from the Reactome Pathways 2024 dataset. |
Episodic ataxia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Episodic kinesigenic dyskinesia 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Episodic kinesigenic dyskinesia 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Episodic kinesigenic dyskinesia 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic kinesigenic dyskinesia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic kinesigenic dyskinesia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic kinesigenic dyskinesia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic ataxia type 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Episodic ataxia type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Episodic hemiplegia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic hemiplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic ataxia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary episodic ataxia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary episodic ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic kinesigenic dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic flaccid weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic flaccid weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic vomiting Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic vomiting phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic memory Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Episodic memory phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Language performance in older adults (adjusted for episodic memory) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Language performance in older adults (adjusted for episodic memory) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Advanced sleep phase syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced sleep phase syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial multiple polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset. |
Familial antiphospholipid syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset. |
Familial Cold Autoinflammatory Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset. |
familial nephrotic syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; hyper-igd syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; hyper-igd syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial cold-induced inflammatory syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
carpal tunnel syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
advanced sleep phase syndrome, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
?familial cold autoinflammatory syndrome 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?familial cold autoinflammatory syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?antiphospholipid syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?antiphospholipid syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
advanced sleep-phase syndrome, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial cold autoinflammatory syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial cold autoinflammatory syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Atypical Mole Melanoma Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Mole Melanoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Sick Sinus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Sick Sinus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Guillain-Barre Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Guillain-Barre Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Telangiectasia And Cancer Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Telangiectasia And Cancer Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hemolytic Uremic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Atypical Hemolytic Uremic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Charge Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Charge Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Factor Deficiency Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Antiphospholipid Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dandy-Walker Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autoinflammatory Syndrome, Familial, Behcet-Like Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autoinflammatory Syndrome, Familial, Behcet-Like in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myelocytic Leukemia-Like Syndrome, Familial, Chronic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myelocytic Leukemia-Like Syndrome, Familial, Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cold Autoinflammatory Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cold Autoinflammatory Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carpal Tunnel Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carpal Tunnel Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Scaphocephaly Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Familial Scaphocephaly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Familial cold autoinflammatory syndrome 3 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial cold autoinflammatory syndrome 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial cold autoinflammatory syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial chylomicronemia syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial chylomicronemia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial nephrotic syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial nephrotic syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial chylomicronemia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial chylomicronemia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial nephrotic syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial woolly hair syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial woolly hair syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial Behcet-like autoinflammatory syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial Behcet-like autoinflammatory syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial cold autoinflammatory syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial cold autoinflammatory syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial multiple polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial idiopathic steroid-resistant nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial cold autoinflammatory syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cold autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial scaphocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial scaphocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial cardiofaciocutaneous syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cardiofaciocutaneous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial Atypical Hemolytic-Uremic Syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Atypical Hemolytic-Uremic Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial steroid-resistant nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial sick sinus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial sick sinus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
repression of pain sensation by the transcriptional regulator dream Gene SetFrom Biocarta Pathways proteins participating in the repression of pain sensation by the transcriptional regulator dream pathway from the Biocarta Pathways dataset. |
Indifference to pain, congenital, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary insensitivity to pain with anhidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary insensitivity to pain with anhidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chronic Pain from the curated CTD Gene-Disease Associations dataset. |
Paroxysmal Extreme Pain Disorder Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset. |
Back Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Back Pain from the curated CTD Gene-Disease Associations dataset. |
Chest Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chest Pain from the curated CTD Gene-Disease Associations dataset. |
Indifference to Pain, Congenital, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Pain, Postoperative Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pain, Postoperative from the curated CTD Gene-Disease Associations dataset. |
Low Back Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Back Pain from the curated CTD Gene-Disease Associations dataset. |
Pain Insensitivity, Congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset. |
Labor Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Labor Pain from the curated CTD Gene-Disease Associations dataset. |
Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pain from the curated CTD Gene-Disease Associations dataset. |
Pain, Intractable Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pain, Intractable from the curated CTD Gene-Disease Associations dataset. |
Nociceptive Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nociceptive Pain from the curated CTD Gene-Disease Associations dataset. |
Abdominal Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abdominal Pain from the curated CTD Gene-Disease Associations dataset. |
Eye Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Pain from the curated CTD Gene-Disease Associations dataset. |
Facial Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Facial Pain from the curated CTD Gene-Disease Associations dataset. |
pain agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pain agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pain disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pain disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ache, low back; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea; opioid-related disorders; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sickle cell; pain; sickle cell anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; pain; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heroin dependence; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heroin dependence; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sickle cell; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
headache; [d]pain in head nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease headache; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
labor pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease labor pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain response Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain tolerance, and opioid addiction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain tolerance, and opioid addiction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain; temporomandibular joint disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; low back pain; scoliosis; spinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complex regional pain syndromes; dystonia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain; pancreatitis, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibromyalgia; hyperalgesia; pain, intractable Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibromyalgia; hyperalgesia; pain, intractable in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temporomandibular joint pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temporomandibular joint pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
musculoskeletal pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease musculoskeletal pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk displacement; low back pain; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; low back pain; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; pain, postoperative Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; pain, postoperative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; postoperative nausea and vomiting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; postoperative nausea and vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk displacement; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; pruritus; pruritus nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; pruritus; pruritus nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibromyalgia; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibromyalgia; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk degeneration; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk degeneration; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos; respiratory insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; postoperative nausea and vomiting; pruritus; pruritus nos; respiratory insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
opioid-related disorders; pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; pain; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; pain; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal pain; dyspepsia; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal pain; dyspepsia; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pain Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term pain in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Neurological pain disorder_Dorsal Root Ganglia_GSE15041 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Neurological pain disorder_Dorsal Root Ganglia_GSE15041 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
behavioral response to pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the behavioral response to pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of chemical stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of chemical stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
sensory perception of pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sensory perception of pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of mechanical stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of mechanical stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of temperature stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of temperature stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2015 dataset. |
Pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
limb pain Gene SetFrom HPO Gene-Disease Associations genes associated with the limb pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mandibular pain Gene SetFrom HPO Gene-Disease Associations genes associated with the mandibular pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chest pain Gene SetFrom HPO Gene-Disease Associations genes associated with the chest pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired pain sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pain sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
back pain Gene SetFrom HPO Gene-Disease Associations genes associated with the back pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal pain Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pain Gene SetFrom HPO Gene-Disease Associations genes associated with the pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low back pain Gene SetFrom HPO Gene-Disease Associations genes associated with the low back pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lower limb pain Gene SetFrom HPO Gene-Disease Associations genes associated with the lower limb pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pain insensitivity Gene SetFrom HPO Gene-Disease Associations genes associated with the pain insensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic pain Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ocular pain Gene SetFrom HPO Gene-Disease Associations genes associated with the ocular pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bone pain Gene SetFrom HPO Gene-Disease Associations genes associated with the bone pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Pain Perception Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain Perception phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Back Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Back Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Chest Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Chest Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pain Threshold Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain Threshold phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pain, Postoperative Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain, Postoperative phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Low Back Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Low Back Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pain Insensitivity, Congenital Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain Insensitivity, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Labor Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Labor Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pelvic Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pelvic Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pain, Intractable Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pain, Intractable phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Complex Regional Pain Syndromes Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Complex Regional Pain Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abdominal Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abdominal Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neck Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neck Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Facial Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Facial Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal pain threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pain threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
paroxysmal extreme pain disorder, 167400, Gene SetFrom OMIM Gene-Disease Associations genes associated with the paroxysmal extreme pain disorder, 167400, phenotype from the curated OMIM Gene-Disease Associations dataset. |
insensitivity to pain, congenital, with anhidrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the insensitivity to pain, congenital, with anhidrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
insensitivity to pain, congenital Gene SetFrom OMIM Gene-Disease Associations genes associated with the insensitivity to pain, congenital phenotype from the curated OMIM Gene-Disease Associations dataset. |
Pain Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pain Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Back Pain, Mechanical Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Back Pain, Mechanical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complex Regional Pain Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complex Regional Pain Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hip Pain Chronic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hip Pain Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Knee Pain Chronic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Knee Pain Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Widespread Chronic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Widespread Chronic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Visceral Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Visceral Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bladder Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bladder Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Pain Insensitivity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Pain Insensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indifference To Pain, Congenital, Autosomal Recessive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indifference To Pain, Congenital, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Neuropathic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Low Back Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myofascial Pain Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myofascial Pain Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paroxysmal Extreme Pain Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paroxysmal Extreme Pain Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Postoperative Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Postoperative Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Deep Pain On Intercourse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deep Pain On Intercourse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Discogenic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Discogenic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prostatic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease With Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Pain Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Onset Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Onset Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cancer Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cancer Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Neuropathic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radiating Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radiating Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inflammatory Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inflammatory Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Moderate Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderate Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chest Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chest Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Temporal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Temporal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nociceptive Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nociceptive Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Knee Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Knee Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Rest Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rest Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Breast Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breast Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Ankle Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Ankle Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Pelvic Pain Of Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Pelvic Pain Of Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hip Joint Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Joint Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hip Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Left Lower Quadrant Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Lower Quadrant Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Wrist Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Wrist in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Lower Quadrant Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Lower Quadrant Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Upper Quadrant Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Upper Quadrant Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shoulder Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Visceral Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Visceral Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mechanical Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mechanical Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bladder Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bladder Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Labor Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Labor Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Post-Stroke Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Post-Stroke Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nerve Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nerve Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Paroxysmal Nerve Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paroxysmal Nerve Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bone Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bone Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Orofacial Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orofacial Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radicular Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radicular Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Pain Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Lower Limb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Lower Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bodily Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bodily Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flank Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flank Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Postoperative Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Postoperative Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Children Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Catch - Finding Of Sensory Dimension Of Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Catch - Finding Of Sensory Dimension Of Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Epigastric Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Epigastric Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Chest Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Chest Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Arm Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Arm Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Renal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteoarticular Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteoarticular Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Incisional Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Incisional Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Spine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chest Pain On Exertion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chest Pain On Exertion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain During Injection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain During Injection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Of Skin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Injection Site Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Injection Site Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intermittent Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Localized Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Localized Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Residual Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Residual Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Jaw Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Jaw Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mandibular Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mandibular Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pleuritic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pleuritic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Knee Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Knee Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Limb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hand Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inguinal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inguinal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Cancer Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Cancer Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Musculoskeletal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Musculoskeletal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Oral Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oral Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Pain Or Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Pain Or Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neurogenic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Pain In Children Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Pain In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cardiac Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonspecific Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonspecific Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Postoperative Hip Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Hip Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Iliac Fossa Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Iliac Fossa Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Sensation Diminished Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Sensation Diminished in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pancreatic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pancreatic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Afterbirth Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Afterbirth Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absence Of Pain Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Back Pain Mechanical Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Back Pain Mechanical in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain After Application Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain After Application in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atypical Chest Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atypical Chest Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Facial Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nipple Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nipple Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Of Uterus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Bladder Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Bladder Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Uncontrolled Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uncontrolled Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Esophagus (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Esophagus (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Breakthrough Cancer Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breakthrough Cancer Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neurological Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurological Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Gastrointestinal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Colicky Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colicky Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Breakthrough Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breakthrough Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unbearable Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unbearable Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retrosternal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retrosternal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Indifference To Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Indifference To Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Pain Score 1 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Pain Score 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Foot Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radiating Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radiating Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dull Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dull Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ear Pain, Ctcae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ear Pain, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deep Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deep Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lower Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Craniofacial Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Craniofacial Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chest Pain On Breathing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chest Pain On Breathing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sciatic Nerve Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sciatic Nerve Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain, Posterior Compartment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain, Posterior Compartment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain, Postural Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain, Postural in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spontaneous Pain Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Pain Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuropathic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Around Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Around Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anal Pain, Ctcae 5 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anal Pain, Ctcae 5 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Scalp Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scalp Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Flank Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Flank Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unilateral Leg Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unilateral Leg Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tumor Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tumor Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Pain Chronic Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Pain Chronic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Of Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Of Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Femur Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Oropharyngeal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oropharyngeal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Excruciating Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Excruciating Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tissue Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tissue Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Post-Thoracotomy Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Post-Thoracotomy Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Intractable Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Intractable Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
behavioral response to acetic acid induced pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the behavioral response to acetic acid induced pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
behavioral response to formalin induced pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the behavioral response to formalin induced pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of mechanical stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of mechanical stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of temperature stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of temperature stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
behavioral response to chemical pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the behavioral response to chemical pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal pain threshold Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pain threshold phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
behavioral response to acetic acid induced pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the behavioral response to acetic acid induced pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
behavioral response to formalin induced pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the behavioral response to formalin induced pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of temperature stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of temperature stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of mechanical stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of mechanical stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of chemical stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of chemical stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
behavioral response to chemical pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the behavioral response to chemical pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of stimulus involved in sensory perception of pain Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of stimulus involved in sensory perception of pain biological process from the curated GO Biological Process Annotations 2025 dataset. |
Paroxysmal extreme pain disorder Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Paroxysmal extreme pain disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Pain agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pain agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pain disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pain disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Paroxysmal extreme pain disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paroxysmal extreme pain disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abnormality of pain sensation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of pain sensation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Paroxysmal extreme pain disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Paroxysmal extreme pain disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Channelopathy-associated congenital insensitivity to pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Channelopathy-associated congenital insensitivity to pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary insensitivity to pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary insensitivity to pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Chest pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Chest pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital Indifference to Pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital Indifference to Pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pain insensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pain insensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Limb pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SCN9A-related neuropathic pain syndromes Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN9A-related neuropathic pain syndromes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Indifference to pain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Indifference to pain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neuropathic pain in type 2 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuropathic pain in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Vaso-occlusive pain in sickle-cell anemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vaso-occlusive pain in sickle-cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fear of pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fear of pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fear of minor pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fear of minor pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Knee pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Knee pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic postoperative pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic postoperative pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Dysmenorrheic pain severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dysmenorrheic pain severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pain medicine use during menstruation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pain medicine use during menstruation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multisite chronic pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multisite chronic pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute post-radiotherapy pain in breast cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute post-radiotherapy pain in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic back pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic back pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to opioid analgesics in cancer (pain decrease) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to opioid analgesics in cancer (pain decrease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Dysmenorrheic pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dysmenorrheic pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neuropathic pain in head and neck cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuropathic pain in head and neck cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Possible neuropathic pain in post total joint replacement surgery for osteoarthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Possible neuropathic pain in post total joint replacement surgery for osteoarthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic widespread musculoskeletal pain Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic widespread musculoskeletal pain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Familial Mediterranean fever Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytosis, benign familial microcytic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign familial neonatal-infantile seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neurofibromatosis, familial spinal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tumoral calcinosis, familial, hyperphosphatemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Febrile seizures, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial restrictive cardiomyopathy 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaze palsy, familial horizontal, with progressive scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hemiplegic migraine type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hemiplegic migraine type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hemiplegic migraine type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions and paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign familial neonatal seizures 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign familial neonatal seizures 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemic nephropathy, familial juvenile, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial cancer of breast Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial benign pemphigus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperpigmentation, familial progressive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial aortopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digital arthropathy-brachydactyly, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Febrile seizures, familial, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial benign hypercalcemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial visceral amyloidosis, Ostertag type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dementia familial British Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial porencephaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
familial hyperinsulinism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinemic hypoglycemia familial 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Febrile seizures, familial, 3b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Paroxysmal familial ventricular fibrillation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypercholesterolemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hidradenitis suppurativa, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dementia, familial Danish Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial intrahepatic cholestasis 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial intrahepatic cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign familial hematuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial heart block type 1A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial heart block type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial dysautonomia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial febrile seizures 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fleck retina, familial benign Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked familial exudative vitreoretinopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial colorectal cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial porphyria cutanea tarda Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial intrahepatic cholestasis 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoclonus, familial cortical Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Migraine, familial basilar Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Breast-ovarian cancer, familial 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercholanemia, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypokalemia-hypomagnesemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenia, limb-girdle, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ventricular fibrillation, paroxysmal familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial platelet disorder with associated myeloid malignancy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial erythrocytosis, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial medullary thyroid carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperlipidemia, familial combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial amyloid polyneuropathy, Iowa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial encephalopathy with neuroserpin inclusion bodies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, familial adult myoclonic, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial myxoma, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, familial partial, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, familial partial, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial juvenile gout Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypobetalipoproteinemia, familial, associated with apob32 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Breast-ovarian cancer, familial 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary familial hypertrophic cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial type 3 hyperlipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tumoral calcinosis, familial, normophosphatemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd8 deficiency, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial infantile myasthenia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked familial atypical mycobacteriosis, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperthyroxinemia, familial dysalbuminemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial type 5 hyperlipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial pulmonary capillary hemangiomatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoalphalipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal hypouricemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoclonic epilepsy, familial infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoplastic, glomerulocystic kidney Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial cold urticaria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic Aneurysm, Familial Abdominal 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset. |
Familial myelofibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset. |
Nephronophthisis, familial juvenile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset. |
Eosinophilia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset. |
Hyperlipidemia, Familial Combined Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset. |
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset. |
Pemphigus, Benign Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, familial visceral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Hypertrophic, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset. |
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Cholestasis, progressive familial intrahepatic 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset. |
Cholestasis, progressive familial intrahepatic 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset. |
Myasthenia, Familial Infantile, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Abdominal 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset. |
STUTTERING, FAMILIAL PERSISTENT, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset. |
Dementia, familial British Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset. |
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Gliosis, Familial Progressive Subcortical Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset. |
CD8 Deficiency, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset. |
Insomnia, Fatal Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset. |
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset. |
Familial HDL deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset. |
Familial dermographism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset. |
Candidiasis, Familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 3 from the curated CTD Gene-Disease Associations dataset. |
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset. |
Erythrocytosis, Familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset. |
Erythrocytosis, Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Visceral Myopathy, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset. |
Hyperthyroidism, Familial Gestational Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset. |
Hematuria, Benign Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset. |
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Migraine, Familial Hemiplegic, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset. |
Cancer, Familial, with In Vitro Radioresistance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Hypoparathyroidism familial isolated Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset. |
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset. |
Hidradenitis suppurativa, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset. |
Dementia, familial Danish Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset. |
Familial medullary thyroid carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset. |
Interstitial Pneumonitis, Desquamative, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Cirrhosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset. |
Familial encephalopathy with neuroserpin inclusion bodies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset. |
Lipodystrophy, Familial Partial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset. |
Familial Mediterranean Fever, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Familial Hypophosphatemic Rickets Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset. |
Keratoacanthoma familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset. |
Hepatic Adenomas, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset. |
Familial Wilms tumor 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset. |
Candidiasis, Familial, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic Hypoglycemia, Familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic Hypoglycemia, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset. |
Familial paroxysmal dystonia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset. |
Atrial fibrillation, familial 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset. |
Hypercholanemia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Hyperbilirubinemia, Transient Familial Neonatal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset. |
Meningioma, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset. |
Dysautonomia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Familial Adult Myoclonic, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset. |
Prostate cancer, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset. |
Convulsions, Benign Familial Infantile, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset. |
Erythrocytosis, Familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset. |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset. |
Hyperthyroxinemia, Familial Dysalbuminemic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Familial cylindromatosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset. |
Familial benign hypercalcemia, type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset. |
Hyperaldosteronism, Familial, Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Atrial myxoma, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset. |
Familial Glucocorticoid Deficiency 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset. |
Tumoral Calcinosis, Normophosphatemic, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset. |
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset. |
Trichoepithelioma multiple familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Periodic fever, familial, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, FAMILIAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset. |
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset. |
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Abdominal 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset. |
Familial schizencephaly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset. |
Neurofibromatosis, Familial Spinal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset. |
Reticuloendotheliosis, familial, with eosinophilia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset. |
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset. |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset. |
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset. |
MITRAL VALVE PROLAPSE, FAMILIAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset. |
Progressive Familial Heart Block, Type Ib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset. |
Familial dilated cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Cholestasis, progressive familial intrahepatic 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset. |
Thymoma, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset. |
Atypical Mycobacteriosis, Familial, X-Linked 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset. |
Familial Testotoxicosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset. |
Hemiplegic migraine, familial type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset. |
Hemiplegic migraine, familial type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset. |
Familial apoceruloplasmin deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset. |
HYPERCHOLESTEROLEMIA, FAMILIAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset. |
Amyloid Neuropathies, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset. |
CANDIDIASIS, FAMILIAL, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset. |
Familial Mediterranean Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset. |
Cerebral Amyloid Angiopathy, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset. |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset. |
Hypobetalipoproteinemia, Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Stuttering, Familial Persistent 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset. |
Trichoepithelioma, Multiple Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Familial Temporal Lobe, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset. |
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset. |
familial mediterranean fever Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial adenomatous polyposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial hyperlipidemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial hemiplegic migraine Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial atrial fibrillation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial lipoprotein lipase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial periodic paralysis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial lipoprotein lipase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial hypertriglyceridemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
benign familial infantile epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial adenomatous polyposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial combined hyperlipidemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial renal oncocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fatal familial insomnia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial mediterranean fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial glomangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial hyperlipidemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial hypercholesterolemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial periodic paralysis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
benign familial neonatal epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial partial lipodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial hemiplegic migraine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial visceral amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial atrial fibrillation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial medullary thyroid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial renal papillary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial retinoblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial adenomatous polyposis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mild familial hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial atypical progressive supranuclear palsy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial or sporadic prostate cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial distal renal tubular acidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial defective apolipoprotein b100. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypercholesterolaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloid neuropathies; amyloid neuropathies, familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early-onset familial alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdomen, acute; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial dysbetalipoproteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial defective apolipoprotein b Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyloid polyneuropathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease (familial) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mild familial hypercholesterolaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial combined hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endogenous hypertriglyceridemia and familial hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial age-related macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial premature myocardial infarction. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
late onset of familial adenomatous polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyloidotic polyneuropathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloid neuropathies, familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperlipidemia, familial combined; mixed hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial defective apolipoprotein b-100 in a chinese man Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature coronary artery disease and familial hypoalphalipoproteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; familial mediterranean fever; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial male-limited precocious puberty. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial combined hyperlipidaemia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; familial mediterranean fever; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial early onset psoriasis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypobetalipoproteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypobetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyotrophic lateral sclerosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyloid polyneuropathy in a hungarian family. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in a hungarian family. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial melanoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rapidly progressive familial amyotrophic lateral sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyotrophic lateral sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypocalciuric hypercalcemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial adenomatous polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hyperinsulinism. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hyperinsulinism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial glucocorticoid deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
late onset familial adenomatous polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyloid polyneuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypercholesterolemia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial partial lipodystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial partial lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial amyloidotic polyneuropathy type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial liver adenomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial liver adenomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer, familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypertrophic cardiomyopathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial cataract Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; atherosclerosis; familial mediterranean fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; atherosclerosis; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial exudative vitreoretinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial exudative vitreoretinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic, familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial dysautonomia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial dysautonomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial alzheimer's disease associated Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
greenland familial cholestasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial diabetes insipidus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial diabetes insipidus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial erythrocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial erythrocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial bronchiectasis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial bronchiectasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial non-ret c cell hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypertension of early onset. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term familial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Parkinson's disease (familial) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
familial hypertriglyceridemia Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
familial atrial fibrillation Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
familial predisposition Gene SetFrom HPO Gene-Disease Associations genes associated with the familial predisposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hyperlipidemia, Familial Combined Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperlipidemia, Familial Combined phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Paralyses, Familial Periodic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Paralyses, Familial Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cardiomyopathy, Hypertrophic, Familial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Familial Mediterranean Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Familial Mediterranean Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lipodystrophy, Familial Partial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lipodystrophy, Familial Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Amyloidosis, Familial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Dysautonomia, Familial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dysautonomia, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Amyloid Neuropathies, Familial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloid Neuropathies, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Insomnia, Fatal Familial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Insomnia, Fatal Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
epilepsy, familial focal, with variable foci Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperparathyroidism, familial primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
{atrial fibrillation, familial, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{breast-ovarian cancer, familial, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
digital arthropathy-brachydactyly, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive familial heart block, type ib Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset. |
migraine, familial basilar Gene SetFrom OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
insomnia, fatal familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
dysautonomia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |