Name

Prinzmetal's variant angina Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prinzmetal's variant angina from the curated CTD Gene-Disease Associations dataset.

angina pectoris; angina, unstable; myocardial infarction; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; angina, unstable; myocardial infarction; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; angina, unstable; coronary artery disease; myocardial infarction; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; angina, unstable; coronary artery disease; myocardial infarction; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

?prinzmetal angina Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?prinzmetal angina phenotype from the curated OMIM Gene-Disease Associations dataset.

angina, unstable; myocardial infarction; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; myocardial infarction; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; myocardial infarction; syndrome; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; myocardial infarction; syndrome; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; coronary thrombosis; inflammation; myocardial infarction; recurrence; syndrome; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; coronary thrombosis; inflammation; myocardial infarction; recurrence; syndrome; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; myocardial infarction; myocardial ischemia; unstable angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; myocardial infarction; myocardial ischemia; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris, variant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris, variant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Angina Pectoris, Variant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Angina Pectoris, Variant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Angina Pectoris Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angina Pectoris from the curated CTD Gene-Disease Associations dataset.

Angina, Unstable Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angina, Unstable from the curated CTD Gene-Disease Associations dataset.

Microvascular Angina Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microvascular Angina from the curated CTD Gene-Disease Associations dataset.

Angina, Stable Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angina, Stable from the curated CTD Gene-Disease Associations dataset.

ludwig's angina Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ludwig's angina in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

angina pectoris; apoplexy; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; apoplexy; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; hyperlipidemias; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; hyperlipidemias; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; hypertension; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; angina; cystatin c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; angina; cystatin c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; stroke; angina; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; stroke; angina; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microvascular angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microvascular angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; angina pectoris; coronary artery disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; angina pectoris; coronary artery disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary spastic angina. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary spastic angina. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; myocardial infarction; obesity; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; myocardial infarction; obesity; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable; coronary stenosis; inflammation; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable; coronary stenosis; inflammation; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; inflammation; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease; inflammation; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomegaly; microvascular angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomegaly; microvascular angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; stable angina of effort Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; stable angina of effort in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; angina pectoris; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; angina pectoris; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary spastic angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary spastic angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; angina Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, vasospastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, vasospastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina, unstable Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina, unstable in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vasospastic angina associated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vasospastic angina associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term angina in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

angina pectoris Gene Set

From HPO Gene-Disease Associations

genes associated with the angina pectoris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Angina Pectoris Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Angina Pectoris phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Microvascular Angina Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Microvascular Angina phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Angina, Unstable Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Angina, Unstable phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Immunodeficiency 18, severe combined immunodeficiency variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 18, severe combined immunodeficiency variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methylmalonic aciduria, cblD type, variant 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methylmalonic aciduria, cblD type, variant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Porphyria, acute intermittent, nonerythroid variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Porphyria, acute intermittent, nonerythroid variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gm2-gangliosidosis, variant b1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, variant b1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria, cblD type, variant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria, cblD type, variant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa, junctional, localisata variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa, junctional, localisata variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rett syndrome, congenital variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, B1 variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, variant type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, variant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotopia, periventricular, Ehlers-Danlos variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotopia, periventricular, Ehlers-Danlos variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, variant AB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oligosaccharyltransferase complex (Stt3A variant) Gene Set

From CORUM Protein Complexes

proteins in the Oligosaccharyltransferase complex (Stt3A variant) protein complex from the CORUM Protein Complexes dataset.

Oligosaccharyltransferase complex (Stt3B variant) Gene Set

From CORUM Protein Complexes

proteins in the Oligosaccharyltransferase complex (Stt3B variant) protein complex from the CORUM Protein Complexes dataset.

CD147-gamma-secretase complex (APH-1a, PS-1, PEN-2, NCT variant) Gene Set

From CORUM Protein Complexes

proteins in the CD147-gamma-secretase complex (APH-1a, PS-1, PEN-2, NCT variant) protein complex from the CORUM Protein Complexes dataset.

Gamma-secretase complex (APH1A, PSEN1, PSENEN, NCSTN variant) Gene Set

From CORUM Protein Complexes

proteins in the Gamma-secretase complex (APH1A, PSEN1, PSENEN, NCSTN variant) protein complex from the CORUM Protein Complexes dataset.

Tay-Sachs Disease, AB Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset.

Vohwinkel Syndrome, Variant Form Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vohwinkel Syndrome, Variant Form from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, Ehlers-Danlos Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Ehlers-Danlos Variant from the curated CTD Gene-Disease Associations dataset.

Carney Complex Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carney Complex Variant from the curated CTD Gene-Disease Associations dataset.

Xeroderma pigmentosum, variant type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma pigmentosum, variant type from the curated CTD Gene-Disease Associations dataset.

RETT SYNDROME, CONGENITAL VARIANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.

eosinophilic variant of chromophobe renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease eosinophilic variant of chromophobe renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cough variant asthma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cough variant asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

variant creutzfeldt-jakob disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease variant creutzfeldt-jakob disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

tall cell variant papillary carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease tall cell variant papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cockayne syndrome or the desanctis-cacchione variant of xeroderma pigmentosum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cockayne syndrome or the desanctis-cacchione variant of xeroderma pigmentosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variant late infantile neuronal ceroid lipofuscinosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

strudwick variant of spondyloepimetaphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease strudwick variant of spondyloepimetaphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variant Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term variant in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

variant MCH Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the variant MCH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Creutzfeldt-Jakob disease (variant) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Creutzfeldt-Jakob disease (variant) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Variant SH3 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Variant SH3 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin E2 variant, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin E2 variant, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

lymphoma/leukemia, b-cell, variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphoma/leukemia, b-cell, variant phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria, cbld type, variant 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria, cbld type, variant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

rett syndrome, congenital variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the rett syndrome, congenital variant phenotype from the curated OMIM Gene-Disease Associations dataset.

maple syrup urine disease, mild variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the maple syrup urine disease, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia, broad bone-platyspondylic variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia, broad bone-platyspondylic variant phenotype from the curated OMIM Gene-Disease Associations dataset.

gm2-gangliosidosis, ab variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the gm2-gangliosidosis, ab variant phenotype from the curated OMIM Gene-Disease Associations dataset.

{creutzfeldt-jakob disease, variant, resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {creutzfeldt-jakob disease, variant, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, variant type Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, variant type phenotype from the curated OMIM Gene-Disease Associations dataset.

rett syndrome, preserved speech variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the rett syndrome, preserved speech variant phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From 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.

ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated OMIM Gene-Disease Associations dataset.

porphyria, acute intermittent, nonerythroid variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the porphyria, acute intermittent, nonerythroid variant phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, cbld type, variant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, cbld type, variant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 18, scid variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 18, scid variant phenotype from the curated OMIM Gene-Disease Associations dataset.

heterotopia, periventricular, ed variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the heterotopia, periventricular, ed variant phenotype from the curated OMIM Gene-Disease Associations dataset.

ebd, localisata variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ebd, localisata variant phenotype from the curated OMIM Gene-Disease Associations dataset.

fabry disease, cardiac variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the fabry disease, cardiac variant phenotype from the curated OMIM Gene-Disease Associations dataset.

carney complex variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the carney complex variant phenotype from the curated OMIM Gene-Disease Associations dataset.