Name

Apparent mineralocorticoid excess Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Apparent mineralocorticoid excess phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Apparent mineralocorticoid excess Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Apparent mineralocorticoid excess from the curated CTD Gene-Disease Associations dataset.

apparent mineralocorticoid excess Gene Set

From OMIM Gene-Disease Associations

genes associated with the apparent mineralocorticoid excess phenotype from the curated OMIM Gene-Disease Associations dataset.

Mineralocorticoid Excess Syndrome, Apparent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mineralocorticoid Excess Syndrome, Apparent from the curated CTD Gene-Disease Associations dataset.

apparent mineralocorticoid excess syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease apparent mineralocorticoid excess syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

apparent beta-hexosaminidase a pseudodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apparent beta-hexosaminidase a pseudodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apparent Gene Set

From GeneRIF Biological Term Annotations

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

Infantile Apparent Life-Threatening Event Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infantile Apparent Life-Threatening Event phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mineralocorticoid deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mineralocorticoid Receptor Antagonists Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Mineralocorticoid Receptor Antagonists from the curated CTD Gene-Chemical Interactions dataset.

mineralocorticoid Gene Set

From GeneRIF Biological Term Annotations

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

mineralocorticoid secretion Gene Set

From GO Biological Process Annotations

genes participating in the mineralocorticoid secretion biological process from the curated GO Biological Process Annotations dataset.

response to mineralocorticoid Gene Set

From GO Biological Process Annotations

genes participating in the response to mineralocorticoid biological process from the curated GO Biological Process Annotations dataset.

cellular response to mineralocorticoid stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to mineralocorticoid stimulus biological process from the curated GO Biological Process Annotations dataset.

mineralocorticoid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mineralocorticoid metabolic process biological process from the curated GO Biological Process Annotations dataset.

mineralocorticoid receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the mineralocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mineralocorticoid secretion Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mineralocorticoid secretion biological process from the curated GO Biological Process Annotations dataset.

regulation of mineralocorticoid secretion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mineralocorticoid secretion biological process from the curated GO Biological Process Annotations dataset.

mineralocorticoid biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the mineralocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

mineralocorticoid receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the mineralocorticoid receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

decreased circulating mineralocorticoid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased circulating mineralocorticoid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating mineralocorticoid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Mineralocorticoid biosynthesis Gene Set

From Reactome Pathways

proteins participating in the Mineralocorticoid biosynthesis pathway from the Reactome Pathways dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, actin, congenital, with excess of thin myofilaments Gene Set

From 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.

Myopathy, congenital, with excess of muscle spindles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disorders of Excessive Somnolence Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disorders of Excessive Somnolence from the curated CTD Gene-Disease Associations dataset.

Myopathy, X-Linked, with Excessive Autophagy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset.

excessive tearing Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked myopathy with excessive autophagy Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

estrogen excess Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

disorders of excessive somnolence; narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorders of excessive somnolence; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aromatase excess syndrome Gene Set

From GAD Gene-Disease Associations

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

disorders of excessive somnolence; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorders of excessive somnolence; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

excessive fat accumulation Gene Set

From GAD Gene-Disease Associations

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

excess Gene Set

From GeneRIF Biological Term Annotations

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

excessive Gene Set

From GeneRIF Biological Term Annotations

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

excessively Gene Set

From GeneRIF Biological Term Annotations

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

reduction of food intake in response to dietary excess Gene Set

From GO Biological Process Annotations

genes participating in the reduction of food intake in response to dietary excess biological process from the curated GO Biological Process Annotations dataset.

response to dietary excess Gene Set

From GO Biological Process Annotations

genes participating in the response to dietary excess biological process from the curated GO Biological Process Annotations dataset.

gonadotropin excess Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the gonadotropin excess phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

adrenocorticotropic hormone excess Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocorticotropic hormone excess phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

excessive wrinkling of palmar skin Gene Set

From HPO Gene-Disease Associations

genes associated with the excessive wrinkling of palmar skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

excessive daytime sleepiness Gene Set

From HPO Gene-Disease Associations

genes associated with the excessive daytime sleepiness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prolactin excess Gene Set

From HPO Gene-Disease Associations

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

thyroid-stimulating hormone excess Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid-stimulating hormone excess phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

excessive salivation Gene Set

From HPO Gene-Disease Associations

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

excessive wrinkled skin Gene Set

From HPO Gene-Disease Associations

genes associated with the excessive wrinkled skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

growth hormone excess Gene Set

From HPO Gene-Disease Associations

genes associated with the growth hormone excess phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadotropin excess Gene Set

From HPO Gene-Disease Associations

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

Anemia, Refractory, with Excess of Blasts Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Refractory, with Excess of Blasts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Disorders of Excessive Somnolence Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Disorders of Excessive Somnolence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

excessive folding of visceral yolk sac Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the excessive folding of visceral yolk sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

excessive digestive secretion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the excessive digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

excessive tearing Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the excessive tearing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

excessive scratching Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the excessive scratching phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

congenital myopathy with excess of muscle spindles Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital myopathy with excess of muscle spindles phenotype from the curated OMIM Gene-Disease Associations dataset.

aromatase excess syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the aromatase excess syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, actin, congenital, with excess of thin myofilaments Gene Set

From 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.

Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP19A1 causes Aromatase excess syndrome (AEXS) pathway from the Reactome Pathways dataset.