| Name |
|---|
Alcohol Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal delirium; alcohol withdrawal seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal delirium; alcohol withdrawal seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol-induced; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol-induced; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
furfuryl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical furfuryl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
3-methylbenzyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 3-methylbenzyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
n-decyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical n-decyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
propargyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical propargyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
isobutyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical isobutyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
tert-Butyl Alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical tert-Butyl Alcohol from the curated CTD Gene-Chemical Interactions dataset. |
crotonyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical crotonyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
patchouli alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical patchouli alcohol from the curated CTD Gene-Chemical Interactions dataset. |
isopentyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical isopentyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
Benzyl Alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Benzyl Alcohol from the curated CTD Gene-Chemical Interactions dataset. |
2-(N-ethylperfluorooctanesulfonamido)ethyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 2-(N-ethylperfluorooctanesulfonamido)ethyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
cinnamyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical cinnamyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
salicyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical salicyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
allyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical allyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
perilla alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical perilla alcohol from the curated CTD Gene-Chemical Interactions dataset. |
Alcohol-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Induced Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset. |
Fetal Alcohol Spectrum Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset. |
ALCOHOL SENSITIVITY, ACUTE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ALCOHOL SENSITIVITY, ACUTE from the curated CTD Gene-Disease Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol Withdrawal Seizures from the curated CTD Gene-Disease Associations dataset. |
Alcohol Drinking Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Alcohol Drinking in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
partial fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol-related birth defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fetal alcohol spectrum disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol abuse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol abuse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol-induced mental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol dependence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol-related neurodevelopmental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
2,3,4,5,6-Pentafluorobenzyl Alcohol Gene Setinteracting proteins for the 2,3,4,5,6-Pentafluorobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
Para-Bromobenzyl Alcohol Gene Setinteracting proteins for the Para-Bromobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
2,4-Difluorobenzyl Alcohol 2,4-Difluoro-1-(Hydroxymethyl)Benzene Gene Setinteracting proteins for the 2,4-Difluorobenzyl Alcohol 2,4-Difluoro-1-(Hydroxymethyl)Benzene drug from the curated DrugBank Drug Targets dataset. |
2,3-Difluorobenzyl Alcohol Gene Setinteracting proteins for the 2,3-Difluorobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
Benzyl alcohol Gene Setinteracting proteins for the Benzyl alcohol drug from the curated DrugBank Drug Targets dataset. |
naltrexone response in alcohol-dependent patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease naltrexone response in alcohol-dependent patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; smoking behavior Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; smoking behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; neuroticism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; cocaine-related disorders; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
suicide, alcohol-dependent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease suicide, alcohol-dependent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol drinking Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol drinking in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; drug dependence; affective psychoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; drug dependence; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; behavior problems Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; behavior problems in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol use Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol use in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; cocaine dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; cocaine dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; nicotine dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; nicotine dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; drug dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; drug dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol consumption Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol consumption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism; disease models, animal; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; disease models, animal; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; cocaine abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; cocaine abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-withdrawal delirium Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-withdrawal delirium in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawl seizure and delirium tremens Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawl seizure and delirium tremens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol associated symptoms; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol associated symptoms; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related polyneuropathy; alcoholic neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related polyneuropathy; alcoholic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease; alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; impulse control disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; impulse control disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; alcoholic psychosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; alcoholic psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders, nervous system; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders, nervous system; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol effects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; prenatal exposure delayed effects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; liver disease, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; liver disease, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-elimination rates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-elimination rates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol withdrawal-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
food and alcohol intake Gene SetFrom GAD Gene-Disease Associations genes associated with the disease food and alcohol intake in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; delirium tremens, alcohol-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; delirium tremens, alcohol-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal delirium; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal delirium; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severity of alcohol dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severity of alcohol dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol elimination Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol elimination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal alcohol syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term alcohol in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Alcohol poisoning_Pancreas_GSE3311 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Alcohol poisoning_Pancreas_GSE3311 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase [nad(p)+] activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase [nad(p)+] activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
cdp-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the cdp-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol o-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol o-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase (nadp+) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase (nadp+) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
fatty-acyl-coa reductase (alcohol-forming) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the fatty-acyl-coa reductase (alcohol-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase (nad) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase (nad) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Alcoholism (alcohol dependence factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (alcohol dependence factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcoholism (12-month weekly alcohol consumption) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (12-month weekly alcohol consumption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcoholism (alcohol use disorder factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (alcohol use disorder factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol dependence (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to alcohol consumption (flushing response) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to alcohol consumption (flushing response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption (transferrin glycosylation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption (transferrin glycosylation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol and nictotine co-dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol and nictotine co-dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption (maxi-drinks) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption (maxi-drinks) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
alcohol abuse Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol abuse in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
alcohol dependence Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol dependence in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
alcohol-induced mental disorder Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Decyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Decyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
5-Hydroxyconiferyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 5-Hydroxyconiferyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
4-Coumaryl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 4-Coumaryl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Propyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Propyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Perillyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Perillyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coniferyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coniferyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Isopropyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Isopropyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Sinapyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Sinapyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Chlordecone alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Chlordecone alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Arachidyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Arachidyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
facial flushing after alcohol intake Gene SetFrom HPO Gene-Disease Associations genes associated with the facial flushing after alcohol intake phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Alcohol-Related Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol-Induced Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Withdrawal Seizures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fetal Alcohol Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Alcohol Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Amnestic Disorder Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Amnestic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Withdrawal Delirium Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Withdrawal Delirium phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol dehydrogenase, iron-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, iron-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-V subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-V subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Quinonprotein alcohol dehydrogenase-like superfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Quinonprotein alcohol dehydrogenase-like superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Quinonprotein alcohol dehydrogenase-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Quinonprotein alcohol dehydrogenase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-IV subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-IV subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vanillyl-alcohol oxidase, C-terminal subdomain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vanillyl-alcohol oxidase, C-terminal subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase superfamily, zinc-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase superfamily, zinc-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase GroES-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase GroES-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CDP-alcohol phosphatidyltransferase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CDP-alcohol phosphatidyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, zinc-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, zinc-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-II subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-II subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
enhanced behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enhanced behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
alcohol preference Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the alcohol preference phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
impaired behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
alcohol aversion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the alcohol aversion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{aerodigestive tract cancer, squamous cell, alcohol-related, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {aerodigestive tract cancer, squamous cell, alcohol-related, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{alcohol dependence, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{alcohol dependence, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
alcohol sensitivity, acute Gene SetFrom OMIM Gene-Disease Associations genes associated with the alcohol sensitivity, acute phenotype from the curated OMIM Gene-Disease Associations dataset. |
{alcohol dependence} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{esophageal cancer, alcohol-related, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {esophageal cancer, alcohol-related, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
phosphotransferases-alcohol-group-acceptor Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term phosphotransferases-alcohol-group-acceptor in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Folate-Alcohol and Cancer Pathway(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Folate-Alcohol and Cancer Pathway(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Alcohol Or Other Drugs Use Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Or Other Drugs Use in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Abuse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Abuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Use Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Use Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetal Alcohol Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Abuse Or Dependence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Abuse Or Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Related Birth Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol-Related Liver Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Related Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Induced Disorders, Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ketoacidosis Due To Acute Alcohol Intoxication Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ketoacidosis Due To Acute Alcohol Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Delirium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Delirium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chlorpropamide-Alcohol Flushing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chlorpropamide-Alcohol Flushing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Related Neurodevelopmental Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Fetal Alcohol Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Alcohol Withdrawal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Alcohol Withdrawal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Toxicity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Toxicity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Alcohol Dependence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Alcohol Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol-Induced Chronic Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Induced Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Dependence With Withdrawal, Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Dependence With Withdrawal, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Alcohol-Induced Mental Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Alcohol-Induced Mental Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uncomplicated Alcohol Withdrawal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uncomplicated Alcohol Withdrawal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Consumption Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hangover From Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hangover From Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hangover From Any Alcohol Or Other Drugs Substance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hangover From Any Alcohol Or Other Drugs Substance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Flush Reaction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Flush Reaction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Problem Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Problem in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Response To Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Response To Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Effect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Effect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity, Acute Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Esophageal Cancer, Alcohol-Related, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Esophageal Cancer, Alcohol-Related, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Facial Flushing After Alcohol Intake Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Flushing After Alcohol Intake in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Craving For Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Craving For Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Dependence, Protection Against Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Dependence, Protection Against in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prenatal Alcohol Exposure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prenatal Alcohol Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Consumption During Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Withdrawal-Induced Major Motor Seizure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Withdrawal-Induced Major Motor Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Status Epilepticus, Alcohol Withdrawal-Induced Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Status Epilepticus, Alcohol Withdrawal-Induced in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Dependence, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Dependence, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2023 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
secondary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
tertiary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tertiary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
tertiary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tertiary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
alcohol dehydrogenase (NADP+) activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase (NADP+) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase (NAD+) activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase [NAD(P)+] activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
CDP-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the CDP-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
enhanced behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alcohol preference Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alcohol preference phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alcohol aversion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alcohol aversion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to alcohol-induced hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to alcohol-induced hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Coniferyl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Coniferyl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
Sinapyl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Sinapyl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
4-Coumaryl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for 4-Coumaryl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
perillyl-alcohol Gene SetFrom LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the perillyl-alcohol small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset. |
salicyl-alcohol Gene SetFrom LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the salicyl-alcohol small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset. |
Folate alcohol and cancer pathway hypotheses Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Folate alcohol and cancer pathway hypotheses pathway from the WikiPathways Pathways 2024 dataset. |
alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2025 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
secondary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
tertiary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tertiary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
tertiary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tertiary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol dehydrogenase (NADP+) activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase (NADP+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol dehydrogenase (NAD+) activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol-forming long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol-forming long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol dehydrogenase [NAD(P)+] activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
CDP-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the CDP-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Alcohol use disorder Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alcohol use disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Metabolic dysfunction and alcohol associated liver disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
alcohol-related birth defects Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-related birth defects in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fetal alcohol spectrum disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol dependence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcohol dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol use disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcohol use disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
alcohol-induced mental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
alcohol-related neurodevelopmental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurobehavioral disorder with prenatal alcohol exposure Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurobehavioral disorder with prenatal alcohol exposure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol sensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alcohol sensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alcohol dependence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alcohol dependence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Problematic alcohol use Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Problematic alcohol use phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (heavy vs. light/non-drinkers) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (heavy vs. light/non-drinkers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Longitudinal alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Longitudinal alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol misuse (trauma interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol misuse (trauma interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spine bone mineral density and alcohol drinking Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spine bone mineral density and alcohol drinking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Problematic alcohol use in trauma-exposed individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Problematic alcohol use in trauma-exposed individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption over the past year Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption over the past year phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption in current drinkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption in current drinkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (drinks per week) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (drinks per week) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (drinkers vs non-drinkers) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (drinkers vs non-drinkers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to alcohol consumption (flushing response) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to alcohol consumption (flushing response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (max-drinks) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (max-drinks) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol and nicotine co-dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol and nicotine co-dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-to-hip circumference ratio (alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cirrhosis (alcohol related) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cirrhosis (alcohol related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Initial alcohol sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Initial alcohol sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (dependence and problematic use scores) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (dependence and problematic use scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (total score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (total score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (consumption score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (consumption score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (12-month weekly alcohol consumption) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (12-month weekly alcohol consumption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (alcohol use disorder factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (alcohol use disorder factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (alcohol dependence factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (alcohol dependence factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial clefts (maternal alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial clefts (maternal alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (transferrin glycosylation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (transferrin glycosylation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Risky sexual behaviors (alcohol dependence interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Risky sexual behaviors (alcohol dependence interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Risky sexual behaviors in alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Risky sexual behaviors in alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence symptom count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence symptom count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Colorectal cancer (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal cancer (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (tolerance) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (tolerance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (desire to cut drinking) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (desire to cut drinking) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (time spent drinking) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (time spent drinking) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial cleft x maternal periconceptional alcohol use interaction (1df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial cleft x maternal periconceptional alcohol use interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Excessive alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Excessive alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol withdrawal symptoms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol withdrawal symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Maximum habitual alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum habitual alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Epigenetic age acceleration in alcohol use disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epigenetic age acceleration in alcohol use disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence or heroin dependence or methamphetamine dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence or heroin dependence or methamphetamine dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol-related hepatocellular carcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol-related hepatocellular carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol drinking status (current drinker vs non-current drinker) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol drinking status (current drinker vs non-current drinker) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
DEHYDRATED ALCOHOL Gene Setinteracting proteins for the DEHYDRATED ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
PHENYLETHYL ALCOHOL Gene Setinteracting proteins for the PHENYLETHYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
ISOPROPYL ALCOHOL Gene Setinteracting proteins for the ISOPROPYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
LAURYL ALCOHOL DIPHOSPHONIC ACID Gene Setinteracting proteins for the LAURYL ALCOHOL DIPHOSPHONIC ACID drug from theDGIdb Drug Targets 2026 dataset. |
PERILLYL ALCOHOL Gene Setinteracting proteins for the PERILLYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
METHYL ALCOHOL Gene Setinteracting proteins for the METHYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
DICHLOROBENZYL ALCOHOL Gene Setinteracting proteins for the DICHLOROBENZYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bethlem myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myofibrillar myopathy, ZASP-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, ZASP-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, centronuclear Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, 3, with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 3, autosomal dominant or recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, early-onset, severe Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, centronuclear, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, myosin storage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, myosin storage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, actin, congenital, with cores Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Minicore myopathy with external ophthalmoplegia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Minicore myopathy with external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Visceral myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Native American myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Native American myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nonaka myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nonaka myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, tubular aggregate, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, tubular aggregate, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myofibrillar myopathy, filamin C-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, filamin C-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy with lactic acidosis, hereditary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe X-linked myotubular myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, actin, congenital, with excess of thin myofilaments Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal myopathy Markesbery-Griggs type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, congenital, with excess of muscle spindles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 2, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary myopathy with early respiratory failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked myopathy with postural muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neutral lipid storage disease with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, congenital, compton-north Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked dominant scapuloperoneal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myofibrillar myopathy 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brody myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nemaline myopathy 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, centronuclear, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal recessive centronuclear myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Miyoshi myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy with tubular aggregates Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital myopathy with fiber type disproportion Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MYOPATHY, CENTRONUCLEAR, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 2 from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, CENTRONUCLEAR, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 1 from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Central Core Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Central Core from the curated CTD Gene-Disease Associations dataset. |
Bethlem myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bethlem myopathy from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Distal, with Anterior Tibial Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset. |
Miyoshi myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi myopathy from the curated CTD Gene-Disease Associations dataset. |
Welander distal myopathy, Swedish type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, MYOFIBRILLAR, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 1 from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, MYOFIBRILLAR, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 4 from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, MYOFIBRILLAR, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 6 from the curated CTD Gene-Disease Associations dataset. |
Nemaline myopathy 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 6 from the curated CTD Gene-Disease Associations dataset. |
Myopathy with lactic acidosis and sideroblastic anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset. |
Nemaline myopathy 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 1 from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Nemaline myopathy 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 5 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. |
Scapuloperoneal Myopathy, X-Linked Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Hyaline Body, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Hyaline Body, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Congenital, Compton-North Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset. |
Myopathy, X-Linked, With Postural Muscle Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset. |
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL MYOPATHY, MYH7-RELATED from the curated CTD Gene-Disease Associations dataset. |
Neutral Lipid Storage Disease with Myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset. |
Distal myopathy, Nonaka type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hereditary Myopathy with Early Respiratory Failure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, SPHEROID BODY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, SPHEROID BODY from the curated CTD Gene-Disease Associations dataset. |
Minicore Myopathy with External Ophthalmoplegia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Minicore Myopathy with External Ophthalmoplegia from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
Myopathy, X-Linked, with Excessive Autophagy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset. |
Myopathy with Lactic Acidosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, CENTRONUCLEAR, X-LINKED Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, X-LINKED from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Myosin Storage Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Myosin Storage from the curated CTD Gene-Disease Associations dataset. |
Nemaline myopathy 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 3 from the curated CTD Gene-Disease Associations dataset. |
Nemaline myopathy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 4 from the curated CTD Gene-Disease Associations dataset. |
Nemaline Myopathy 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 2 from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy 3, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Inclusion body myopathy autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion body myopathy autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Brody myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brody myopathy from the curated CTD Gene-Disease Associations dataset. |
Nemaline Myopathy 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 7 from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset. |
mitochondrial myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
brody myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease brody myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bethlem myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bethlem myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
nemaline myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease nemaline myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
central core myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central core myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital structural myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
centronuclear myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease centronuclear myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
myopathy of extraocular muscle Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy of extraocular muscle from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
myopathy Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
congenital structural myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central core myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central core myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brody myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
myopathy of extraocular muscle Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mitochondrial myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bethlem myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
x-linked myopathy with excessive autophagy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
centronuclear myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
nemaline myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adult onset multi/minicore myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
variable myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease variable myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mild myotubular myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mild myotubular myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inherited myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inherited myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mitochondrial myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nemaline myopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nemaline myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myopathy, idiopathic inflammatory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myopathy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term myopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
myopathy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease myopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
scapuloperoneal myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the scapuloperoneal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
myofibrillar myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the myofibrillar myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mitochondrial myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skeletal myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the skeletal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
minicore (multicore) myopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the minicore (multicore) myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
myopathy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the myopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
nemaline myopathy 6, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, spheroid body Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, spheroid body phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy with extrapyramidal signs Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy with extrapyramidal signs phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, early-onset, with fatal cardiomyopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset. |
centronuclear myopathy 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the centronuclear myopathy 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myosin storage Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myosin storage phenotype from the curated OMIM Gene-Disease Associations dataset. |
native american myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the native american myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
inclusion body myopathy, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the inclusion body myopathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, x-linked, with postural muscle atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 1, autosomal dominant or recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, tubular aggregate Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, tubular aggregate phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, with myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 8, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 8, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 4, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
brody myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the brody myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
neutral lipid storage disease with myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutral lipid storage disease with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, actin, congenital, with cores Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with cores phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, congenital, with fiber-type disproportion, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
?myopathy, congenital, compton-north Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?myopathy, congenital, compton-north phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy with lactic acidosis, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy with lactic acidosis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 5, amish type Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 5, amish type phenotype from the curated OMIM Gene-Disease Associations dataset. |
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, reducing body, x-linked, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital myopathy with excess of muscle spindles Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital myopathy with excess of muscle spindles phenotype from the curated OMIM Gene-Disease Associations dataset. |
welander distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
bethlem myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the bethlem myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, centronuclear, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, proximal, with early respiratory muscle involvement Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset. |
laing distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, congenital, with fiber-type disproportion 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?myopathy, tubular aggregate, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?myopathy, tubular aggregate, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
scapuloperoneal myopathy, x-linked dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 7, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
mitochondrial myopathy and sideroblastic anemia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the mitochondrial myopathy and sideroblastic anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myotubular myopathy, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the myotubular myopathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 3, autosomal dominant or recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
minicore myopathy with external ophthalmoplegia Gene SetFrom OMIM Gene-Disease Associations genes associated with the minicore myopathy with external ophthalmoplegia phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, with anterior tibial onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
cap myopathy 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cap myopathy 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cap myopathy 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cap myopathy 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{centronuclear myopathy, autosomal, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {centronuclear myopathy, autosomal, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, congenital, with fiber-type disproportion Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion phenotype from the curated OMIM Gene-Disease Associations dataset. |
inclusion body myopathy-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the inclusion body myopathy-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, centronuclear, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, centronuclear, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, centronuclear Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear phenotype from the curated OMIM Gene-Disease Associations dataset. |
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, reducing body, x-linked, severe early-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 2, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy due to cpt ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
nonaka myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the nonaka myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, tateyama type Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset. |
visceral myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the visceral myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, actin, congenital, with excess of thin myofilaments Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated OMIM Gene-Disease Associations dataset. |
nemaline myopathy 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the nemaline myopathy 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy due to myoadenylate deaminase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Inclusion Body Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neutral Lipid Storage Disease With Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neutral Lipid Storage Disease With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Core Myopathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Core Myopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Centronuclear Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
X-Linked Centronuclear Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Actin-Accumulation Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Actin-Accumulation Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Myotubular Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Myotubular Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Centronuclear Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cap Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Structural Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Structural Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intranuclear Rod Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intranuclear Rod Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myofibrillar Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myofibrillar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nemaline Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nemaline Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonaka Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonaka Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scapuloperoneal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tubular Aggregate Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tubular Aggregate Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vacuolar Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vacuolar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Zebra Body Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Zebra Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Visceral Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Visceral Myopathy, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Miyoshi Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bethlem Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bethlem Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Minicore Myopathy With External Ophthalmoplegia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Minicore Myopathy With External Ophthalmoplegia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multi-Core Congenital Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multi-Core Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scapuloperoneal Myopathy, X-Linked Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sarcoid Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sarcoid Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brody Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brody Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myotubular (Centronuclear) Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myotubular (Centronuclear) Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Axial Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Axial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Critical Illness Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Critical Illness Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Welander Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Necrotizing Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Myopathy With Focal Depletion Of Mitochondria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, With Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autoimmune Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Congenital Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing-Body Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing-Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Myopathy With Early Respiratory Failure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Myopathy With Early Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Native American Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Native American Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oculopharyngodistal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngodistal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Limb-Girdle Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyglucosan Body Myopathy 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Klhl9-Related Early-Onset Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myotubular Myopathy With Abnormal Genital Development Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myotubular Myopathy With Abnormal Genital Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Myopathy 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inflammatory Myopathy With Abundant Macrophages Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Myopathy With Abundant Macrophages in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inclusion Body Myopathy, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spheroid Body Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spheroid Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Myopathy With Lactic Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy With Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyglucosan Body Myopathy Type 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Samaritan Congenital Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Samaritan Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Myopathy With Myasthenic-Like Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myopathy With Myasthenic-Like Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Desmin Related Myopathy With Mallory Body-Like Inclusions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Desmin Related Myopathy With Mallory Body-Like Inclusions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cap Myopathy 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cap Myopathy, Tpm2-Related Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm2-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cap Myopathy, Tpm3-Related (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm3-Related (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
myopathy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the myopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Nemaline myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Mitochondrial myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mitochondrial myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myofibrillar myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
GNE myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease GNE myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital structural myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital structural myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Centronuclear myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital myopathy 4A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 4A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myofibrillar myopathy 9 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy 9 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital myopathy 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Native American myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Native American myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hyaline body myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyaline body myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Brody myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Brody myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital myopathy 1B Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Nemaline myopathy 3 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital myopathy 1A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Centronuclear myopathy X-linked Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy X-linked from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myopathy Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
COX deficiency, infantile mitochondrial myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mitochondrial myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital structural myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
GNE myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease GNE myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy X-linked Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy X-linked in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Oculopharyngodistal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fatal infantile hypertonic myofibrillar myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with rimmed vacuoles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
COX deficiency, benign infantile mitochondrial myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked myopathy with excessive autophagy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 1A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bethlem myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant centronuclear myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with anterior tibial onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Compton-North congenital myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Compton-North congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Scapuloperoneal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyaline body myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 1B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
myopathy, lactic acidosis, and sideroblastic anemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy 6 with fiber-type disproportion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 6 with fiber-type disproportion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Brody myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cylindrical spirals myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cylindrical spirals myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 4A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 11 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myopathy with extrapyramidal signs Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy with extrapyramidal signs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive centronuclear myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Isolated mitochondrial myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 5A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Native American myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Native American myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Centronuclear myopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Oculopharyngodistal myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myofibrillar myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myopathy of extraocular muscle Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 22A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Tubular aggregate myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tubular aggregate myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant hyaline body myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nemaline myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital myopathy 22B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive hyaline body myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myopathy caused by variation in F Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in F phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SELENON-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SELENON-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myofibrillar myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Centronuclear myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SCN4A-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN4A-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
GNE myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the GNE myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant centronuclear myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe X-linked myotubular myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sarcotubular myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sarcotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inclusion body myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TPM3-related core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM3-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nemaline myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nemaline myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital multicore myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital multicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
RYR1-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the RYR1-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MYH7-related skeletal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH7-related skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myosin storage myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myosin storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Visceral myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Desmin-related myofibrillar myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Desmin-related myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bethlem myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Collagen 6-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Collagen 6-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Batten-Turner congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Batten-Turner congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brody myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inborn mitochondrial myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Actin accumulation myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Actin accumulation myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital myopathy 2b Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital myopathy 2c Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2c phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive scapulohumeroperoneal distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital myopathy 10b Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 10b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MEGF10-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MEGF10-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MYPN-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MYPN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neutral lipid storage myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral lipid storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Welander distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fatal infantile hypertonic myofibrillar myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Scapuloperoneal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intellectual disability and myopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and myopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TTN-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TTN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myopathy caused by variation in POMG Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in POMG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bailey-Bloch congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bailey-Bloch congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Metabolic myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiminicore myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiminicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Miyoshi myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myopathy caused by variation in PO Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in PO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Compton-North congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Compton-North congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Metabolic myopathy due to lactate transporter defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary inclusion-body myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion-body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polyglucosan body myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polyglucosan body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant mitochondrial myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
HNRNPDL-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the HNRNPDL-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Axial myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Axial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SGCG-related congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SGCG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mitochondrial myopathy-lactic acidosis-deafness syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-lactic acidosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
CAP-congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the CAP-congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ACTA1 gene related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTA1 gene related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mitochondrial myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Myopathy due to calsequestrin and SERCA1 protein overload Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin and SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital nonprogressive myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nonprogressive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyaline body myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyaline body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TPM2-related cap myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related cap myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MYH2-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inclusion body myopathy and brain white matter abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy and brain white matter abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital structural myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital structural myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood-onset autosomal recessive myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skeletal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TPM2-related myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive centronuclear myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial idiopathic inflammatory myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
COL6A2-related core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the COL6A2-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finnish upper limb-onset distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SPEG-related congenital myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SPEG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
IDUA-related core myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the IDUA-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Oculopharyngodistal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Oculopharyngodistal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Simvastatin-induced myopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Simvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Atorvastatin-induced myopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atorvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Statin-induced myopathy (severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Statin-induced myopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic inflammatory myopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |