Name

Amelogenesis Imperfecta, Type Ic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Type Ic from the curated CTD Gene-Disease Associations dataset.

amelogenesis imperfecta, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AMELOGENESIS IMPERFECTA, TYPE IH Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMELOGENESIS IMPERFECTA, TYPE IH phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amelogenesis imperfecta, hypocalcification type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amelogenesis imperfecta, hypocalcification type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amelogenesis imperfecta pigmented hypomaturation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amelogenesis imperfecta pigmented hypomaturation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amelogenesis Imperfecta, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Type III from the curated CTD Gene-Disease Associations dataset.

Amelogenesis Imperfecta, Type IV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Type IV from the curated CTD Gene-Disease Associations dataset.

Amelogenesis Imperfecta, Hypomaturation Type, Iia2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Hypomaturation Type, Iia2 from the curated CTD Gene-Disease Associations dataset.

Amelogenesis Imperfecta, Hypomaturation Type, Iia3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Hypomaturation Type, Iia3 from the curated CTD Gene-Disease Associations dataset.

Amelogenesis Imperfecta, Type IB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis Imperfecta, Type IB from the curated CTD Gene-Disease Associations dataset.

Amelogenesis imperfecta pigmented hypomaturation type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis imperfecta pigmented hypomaturation type from the curated CTD Gene-Disease Associations dataset.

amelogenesis imperfecta, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type ig (enamel-renal syndrome) Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type ig (enamel-renal syndrome) phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type iia5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iia5 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type iia3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iia3 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type iia2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iia2 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type iia1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iia1 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta type, iia4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta type, iia4 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

Amelogenesis imperfecta - hypoplastic autosomal dominant - local Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amelogenesis imperfecta - hypoplastic autosomal dominant - local phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy amelogenesis imperfecta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amelogenesis Imperfecta Gene Set

From CTD Gene-Disease Associations

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

Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 from the curated CTD Gene-Disease Associations dataset.

AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 from the curated CTD Gene-Disease Associations dataset.

amelogenesis imperfecta Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease amelogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

amelogenesis imperfecta Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amelogenesis imperfecta Gene Set

From HPO Gene-Disease Associations

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

Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like Gene Set

From OMIM Gene-Disease Associations

genes associated with the exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like phenotype from the curated OMIM Gene-Disease Associations dataset.

Osteogenesis imperfecta type 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dentinogenesis imperfecta - Shield's type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dentinogenesis imperfecta - Shield's type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta Levin type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta Levin type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

OSTEOGENESIS IMPERFECTA, TYPE IIC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the OSTEOGENESIS IMPERFECTA, TYPE IIC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 2, thin-bone Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 2, thin-bone phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta, type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis imperfecta, type 2A from the curated CTD Gene-Disease Associations dataset.

Osteogenesis imperfecta, type 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis imperfecta, type 7 from the curated CTD Gene-Disease Associations dataset.

Osteogenesis imperfecta, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis imperfecta, type 3 from the curated CTD Gene-Disease Associations dataset.

Osteogenesis Imperfecta, Type IX Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis Imperfecta, Type IX from the curated CTD Gene-Disease Associations dataset.

Osteogenesis imperfecta, type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis imperfecta, type 4 from the curated CTD Gene-Disease Associations dataset.

Osteogenesis imperfecta, type VIII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteogenesis imperfecta, type VIII from the curated CTD Gene-Disease Associations dataset.

Dentinogenesis imperfecta, shields type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dentinogenesis imperfecta, shields type 3 from the curated CTD Gene-Disease Associations dataset.

dentinogenesis imperfecta, shields type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentinogenesis imperfecta, shields type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type viii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type vii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type xi Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type xi phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type xv Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type xv phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type xiii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type xiii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type xiv Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type xiv phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type xii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type xii phenotype from the curated OMIM Gene-Disease Associations dataset.

dentinogenesis imperfecta, shields type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentinogenesis imperfecta, shields type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type ix Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type x Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteogenesis imperfecta, type x phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis Gene Set

From GeneRIF Biological Term Annotations

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

amelogenesis Gene Set

From GO Biological Process Annotations

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

Hereditary cerebral amyloid angiopathy, Icelandic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harlequin type ichthyosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Harlequin type ichthyosis from the curated CTD Gene-Disease Associations dataset.

Lamellar ichthyosis, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lamellar ichthyosis, type 2 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis hystrix, Curth Macklin type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis hystrix, Curth Macklin type from the curated CTD Gene-Disease Associations dataset.

Lamellar ichthyosis, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lamellar ichthyosis, type 3 from the curated CTD Gene-Disease Associations dataset.

ichthyosis histrix, curth-macklin type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis histrix, curth-macklin type phenotype from the curated OMIM Gene-Disease Associations dataset.

Osteogenesis imperfecta with normal sclerae, dominant form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta with normal sclerae, dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta, recessive perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta, recessive perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 from the curated CTD Gene-Disease Associations dataset.

Osteogenesis Imperfecta Gene Set

From CTD Gene-Disease Associations

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

Dentinogenesis Imperfecta Gene Set

From CTD Gene-Disease Associations

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

osteogenesis imperfecta Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease osteogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

dentinogenesis imperfecta Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease dentinogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fibrogenesis imperfecta ossium Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dentinogenesis imperfecta Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

osteogenesis imperfecta Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hearing loss/deafness; osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

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

osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

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

imperfecta Gene Set

From GeneRIF Biological Term Annotations

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

dentinogenesis imperfecta Gene Set

From HPO Gene-Disease Associations

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

Osteogenesis Imperfecta Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

X-linked ichthyosis with steryl-sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bullous ichthyosiform erythroderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bullous ichthyosiform erythroderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Triglyceride storage disease with ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lamellar ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lamellar ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis prematurity syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis prematurity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

maml1-rbp-jkappa- icn1 complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the maml1-rbp-jkappa- icn1 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

icosahedral viral capsid Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the icosahedral viral capsid cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ITGA2B-ITGB3-ICAM4 complex Gene Set

From CORUM Protein Complexes

proteins in the ITGA2B-ITGB3-ICAM4 complex protein complex from the CORUM Protein Complexes dataset.

ITGAV-ITGB5-ICAM4 complex Gene Set

From CORUM Protein Complexes

proteins in the ITGAV-ITGB5-ICAM4 complex protein complex from the CORUM Protein Complexes dataset.

Itgax-Itgb2-Icam4 complex Gene Set

From CORUM Protein Complexes

proteins in the Itgax-Itgb2-Icam4 complex protein complex from the CORUM Protein Complexes dataset.

P12-ICHIKAWA Gene Set

From COSMIC Cell Line Gene CNV Profiles

genes with high or low copy number in P12-ICHIKAWA relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.

P12-ICHIKAWA Gene Set

From COSMIC Cell Line Gene Mutation Profiles

genes mutated in the P12-ICHIKAWA cell line from the COSMIC Cell Line Gene Mutation Profiles dataset.

3,7-bis(2-hydroxyethyl)icaritin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 3,7-bis(2-hydroxyethyl)icaritin from the curated CTD Gene-Chemical Interactions dataset.

ICI 192605 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 192605 from the curated CTD Gene-Chemical Interactions dataset.

icaritin Gene Set

From CTD Gene-Chemical Interactions

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

icariin Gene Set

From CTD Gene-Chemical Interactions

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

ICI 211965 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 211965 from the curated CTD Gene-Chemical Interactions dataset.

icajine Gene Set

From CTD Gene-Chemical Interactions

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

ICI 199441 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 199441 from the curated CTD Gene-Chemical Interactions dataset.

ICI 118551 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 118551 from the curated CTD Gene-Chemical Interactions dataset.

IC486241 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical IC486241 from the curated CTD Gene-Chemical Interactions dataset.

ICI D2138 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI D2138 from the curated CTD Gene-Chemical Interactions dataset.

ICI 164384 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 164384 from the curated CTD Gene-Chemical Interactions dataset.

icilin Gene Set

From CTD Gene-Chemical Interactions

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

ICI 198615 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 198615 from the curated CTD Gene-Chemical Interactions dataset.

ICI 89406 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ICI 89406 from the curated CTD Gene-Chemical Interactions dataset.

icatibant Gene Set

From CTD Gene-Chemical Interactions

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

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Ichthyosis with hypotrichosis, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis with hypotrichosis, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Lamellar, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Lamellar, 5 from the curated CTD Gene-Disease Associations dataset.

Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis from the curated CTD Gene-Disease Associations dataset.

Ichthyosis Bullosa of Siemens Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis Bullosa of Siemens from the curated CTD Gene-Disease Associations dataset.

Ichthyosis Vulgaris Gene Set

From CTD Gene-Disease Associations

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

ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis follicularis atrichia photophobia syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis follicularis atrichia photophobia syndrome from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Lamellar Gene Set

From CTD Gene-Disease Associations

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

Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.

Ichthyosis Gene Set

From CTD Gene-Disease Associations

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

ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR from the curated CTD Gene-Disease Associations dataset.

Ichthyosis prematurity syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis prematurity syndrome from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, X-Linked Gene Set

From CTD Gene-Disease Associations

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

congenital ichthyosiform erythroderma Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital ichthyosiform erythroderma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital ichthyosiform erythroderma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked ichthyosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ichthyosis vulgaris Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

parasitic ichthyosporea infectious disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Icodextrin Gene Set

From DrugBank Drug Targets

interacting proteins for the Icodextrin drug from the curated DrugBank Drug Targets dataset.

Icosapent Gene Set

From DrugBank Drug Targets

interacting proteins for the Icosapent drug from the curated DrugBank Drug Targets dataset.

iCo-007 Gene Set

From DrugBank Drug Targets

interacting proteins for the iCo-007 drug from the curated DrugBank Drug Targets dataset.

Icatibant Gene Set

From DrugBank Drug Targets

interacting proteins for the Icatibant drug from the curated DrugBank Drug Targets dataset.

ICA-105665 Gene Set

From DrugBank Drug Targets

interacting proteins for the ICA-105665 drug from the curated DrugBank Drug Targets dataset.

IC261 Gene Set

From DrugBank Drug Targets

interacting proteins for the IC261 drug from the curated DrugBank Drug Targets dataset.

4-[(10s,14s,18s)-18-(2-Amino-2-Oxoethyl)-14-(1-Naphthylmethyl)-8,17,20-Trioxo-7,16,19-Triazaspiro[5.14]Icos-11-En-10-Yl]Benzylphosphonic Acid Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-[(10s,14s,18s)-18-(2-Amino-2-Oxoethyl)-14-(1-Naphthylmethyl)-8,17,20-Trioxo-7,16,19-Triazaspiro[5.14]Icos-11-En-10-Yl]Benzylphosphonic Acid drug from the curated DrugBank Drug Targets dataset.

icterophyloric syndrome Gene Set

From GAD Gene-Disease Associations

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

soluble icam-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease soluble icam-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; hepatitis c, chronic; icterus; jaundice Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; hepatitis c, chronic; icterus; jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ichthyosis Gene Set

From GAD Gene-Disease Associations

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

ichthyosis vulgaris Gene Set

From GAD Gene-Disease Associations

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

hepatitis c; icterus; jaundice Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; icterus; jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatitis, atopic; ichthyosis vulgaris Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, atopic; ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ichthyosis, x-linked Gene Set

From GAD Gene-Disease Associations

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

lamellar ichthyosis Gene Set

From GAD Gene-Disease Associations

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

disease models, animal; ichthyosiform erythroderma, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease models, animal; ichthyosiform erythroderma, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ichthyosiform erythroderma, congenital Gene Set

From GAD Gene-Disease Associations

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

dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, allergic contact; hypersensitivity; hypersensitivity, immediate; ichthyosis vulgaris in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

P12-ICHIKAWA Gene Set

From GDSC Cell Line Gene Expression Profiles

genes with high or low expression in P12-ICHIKAWA relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.

icldn Gene Set

From GeneRIF Biological Term Annotations

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

icil1ra1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icil1ra1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ictal Gene Set

From GeneRIF Biological Term Annotations

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

ic50s Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ic50s in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icbp90 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icbp90 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icos Gene Set

From GeneRIF Biological Term Annotations

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

icam1vcam1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1vcam1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

iclinduced Gene Set

From GeneRIF Biological Term Annotations

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

icosb7h Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icosb7h in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icoslicos Gene Set

From GeneRIF Biological Term Annotations

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

icodextrin Gene Set

From GeneRIF Biological Term Annotations

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

ic53 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ic53 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ic50 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ic50 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam4mediated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam4mediated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp22 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp22 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp27 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp27 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1intercellular Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1intercellular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icds Gene Set

From GeneRIF Biological Term Annotations

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

iclstalled Gene Set

From GeneRIF Biological Term Annotations

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

icmediated Gene Set

From GeneRIF Biological Term Annotations

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

icam3dcsign Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam3dcsign in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ick Gene Set

From GeneRIF Biological Term Annotations

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

ici Gene Set

From GeneRIF Biological Term Annotations

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

ich Gene Set

From GeneRIF Biological Term Annotations

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

icm Gene Set

From GeneRIF Biological Term Annotations

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

icl Gene Set

From GeneRIF Biological Term Annotations

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

ica Gene Set

From GeneRIF Biological Term Annotations

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

icf Gene Set

From GeneRIF Biological Term Annotations

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

ice Gene Set

From GeneRIF Biological Term Annotations

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

icd Gene Set

From GeneRIF Biological Term Annotations

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

ics Gene Set

From GeneRIF Biological Term Annotations

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

icr Gene Set

From GeneRIF Biological Term Annotations

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

icp Gene Set

From GeneRIF Biological Term Annotations

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

icu Gene Set

From GeneRIF Biological Term Annotations

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

ickrelated Gene Set

From GeneRIF Biological Term Annotations

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

icoslg Gene Set

From GeneRIF Biological Term Annotations

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

icc Gene Set

From GeneRIF Biological Term Annotations

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

icytochrome Gene Set

From GeneRIF Biological Term Annotations

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

icospositive Gene Set

From GeneRIF Biological Term Annotations

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

icam5 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam5 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam4 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam4 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ictp Gene Set

From GeneRIF Biological Term Annotations

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

iceland Gene Set

From GeneRIF Biological Term Annotations

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

icn1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icn1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icb1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icb1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ich1lsinduced Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ich1lsinduced in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icap1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icap1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icap1modulated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icap1modulated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam2fc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam2fc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1and Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1and in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam3grabbing Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam3grabbing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icv Gene Set

From GeneRIF Biological Term Annotations

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

iccs Gene Set

From GeneRIF Biological Term Annotations

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

icln159 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icln159 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ichthyin Gene Set

From GeneRIF Biological Term Annotations

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

ica1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ica1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ical Gene Set

From GeneRIF Biological Term Annotations

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

icap1alpha Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icap1alpha in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1transfected Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1transfected in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icreased Gene Set

From GeneRIF Biological Term Annotations

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

ic3bopsonized Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ic3bopsonized in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icotinib Gene Set

From GeneRIF Biological Term Annotations

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

icmt Gene Set

From GeneRIF Biological Term Annotations

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

icaritin Gene Set

From GeneRIF Biological Term Annotations

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

icosl Gene Set

From GeneRIF Biological Term Annotations

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

icthyosis Gene Set

From GeneRIF Biological Term Annotations

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

ichthyosiform Gene Set

From GeneRIF Biological Term Annotations

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

icam2alphaactininactin Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam2alphaactininactin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icol Gene Set

From GeneRIF Biological Term Annotations

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

ic3b Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ic3b in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ica512 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ica512 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icsbpirf8 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icsbpirf8 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1beta2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1beta2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ici182780 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ici182780 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ichthyoses Gene Set

From GeneRIF Biological Term Annotations

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

icrf193 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icrf193 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp0mediated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp0mediated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icr1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icr1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icami Gene Set

From GeneRIF Biological Term Annotations

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

icam1expressing Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1expressing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icln Gene Set

From GeneRIF Biological Term Annotations

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

icls Gene Set

From GeneRIF Biological Term Annotations

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

icl2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icl2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icl3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icl3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1lfa1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1lfa1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1crp Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1crp in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icpp Gene Set

From GeneRIF Biological Term Annotations

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

icsi Gene Set

From GeneRIF Biological Term Annotations

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

icat Gene Set

From GeneRIF Biological Term Annotations

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

icam Gene Set

From GeneRIF Biological Term Annotations

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

icad Gene Set

From GeneRIF Biological Term Annotations

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

icam4alphavbeta3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam4alphavbeta3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icsbp Gene Set

From GeneRIF Biological Term Annotations

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

ickmakmok Gene Set

From GeneRIF Biological Term Annotations

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

icelandic Gene Set

From GeneRIF Biological Term Annotations

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

icariin Gene Set

From GeneRIF Biological Term Annotations

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

iconverting Gene Set

From GeneRIF Biological Term Annotations

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

icrac Gene Set

From GeneRIF Biological Term Annotations

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

ich1ced3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ich1ced3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ica69 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ica69 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icercrem Gene Set

From GeneRIF Biological Term Annotations

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

ichthyosis Gene Set

From GeneRIF Biological Term Annotations

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

icos1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icos1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ictev Gene Set

From GeneRIF Biological Term Annotations

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

icvd Gene Set

From GeneRIF Biological Term Annotations

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

icp22dependent Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp22dependent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1stimulated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1stimulated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icyp11b1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icyp11b1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icinduced Gene Set

From GeneRIF Biological Term Annotations

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

icam1activated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1activated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1r Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1r in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam3fc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam3fc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1driven Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1driven in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icsbp1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icsbp1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp4 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp4 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp6 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp6 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icp0 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icp0 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icer Gene Set

From GeneRIF Biological Term Annotations

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

icr62 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icr62 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icarisidemediated Gene Set

From GeneRIF Biological Term Annotations

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

ica27243 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ica27243 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1dependent Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1dependent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icam1binding Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term icam1binding in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

icponull Gene Set

From GeneRIF Biological Term Annotations

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

icSARA deltaORF6_12Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_12Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_60Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_60Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_0Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_0Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_36Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_36Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_36Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_36Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_0Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_0Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_7Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_7Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS-Cov_Day1_None_GSE50000 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS-Cov_Day1_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_72Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_72Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_54Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_54Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_48Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_48Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_36Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_36Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_72Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_72Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_12Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_12Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_3Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_3Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_24Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_24Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_30Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_30Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS-Cov_Day7_None_GSE50000 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS-Cov_Day7_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_54Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_54Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_7Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_7Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_60Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_60Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_24Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_24Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_72Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_72Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS-Cov_Day2_None_GSE50000 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS-Cov_Day2_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_30Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_30Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_0Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_0Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_7Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_7Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_48Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_48Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_30Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_30Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS-Cov_Day4_None_GSE50000 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS-Cov_Day4_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARA deltaORF6_24Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARA deltaORF6_24Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_48Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_48Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_60Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_60Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_54Hour_None_GSE37827 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_54Hour_None_GSE37827 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_12Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_12Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icSARS CoV_3Hour_23365422_GSE33267 Gene Set

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the icSARS CoV_3Hour_23365422_GSE33267 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

icosanoid transport Gene Set

From GO Biological Process Annotations

genes participating in the icosanoid transport biological process from the curated GO Biological Process Annotations dataset.

icosanoid secretion Gene Set

From GO Biological Process Annotations

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

negative regulation of icosanoid secretion Gene Set

From GO Biological Process Annotations

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

icosanoid biosynthetic process Gene Set

From GO Biological Process Annotations

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

regulation of icosanoid secretion Gene Set

From GO Biological Process Annotations

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

icosanoid catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the icosanoid catabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of icosanoid secretion Gene Set

From GO Biological Process Annotations

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

icosanoid metabolic process Gene Set

From GO Biological Process Annotations

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

maml1-rbp-jkappa- icn1 complex Gene Set

From GO Cellular Component Annotations

proteins localized to the maml1-rbp-jkappa- icn1 complex cellular component from the curated GO Cellular Component Annotations dataset.

5(s)-hydroxyperoxy-6e,8z,11z,14z-icosatetraenoic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the 5(s)-hydroxyperoxy-6e,8z,11z,14z-icosatetraenoic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

icosanoid binding Gene Set

From GO Molecular Function Annotations

genes performing the icosanoid binding molecular function from the curated GO Molecular Function Annotations dataset.

icosatetraenoic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the icosatetraenoic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

5-hydroxy-6e,8z,11z,14z-icosatetraenoic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the 5-hydroxy-6e,8z,11z,14z-icosatetraenoic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

icosanoid receptor activity Gene Set

From GO Molecular Function Annotations

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

icosanoid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the icosanoid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

icam-3 receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the icam-3 receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

5-oxo-6e,8z,11z,14z-icosatetraenoic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the 5-oxo-6e,8z,11z,14z-icosatetraenoic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

[3H]ICI-198615 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [3H]ICI-198615 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[des-Arg10]icatibant Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [des-Arg10]icatibant ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

icatibant Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

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

ICI 192605 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI 192605 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ICI 118551 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI 118551 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ICI 169369 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI 169369 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ICI 174 864 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI 174 864 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ICI 204448 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI 204448 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ICI198615 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ICI198615 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I](-)ICYP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I](-)ICYP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I]ICYP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I]ICYP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

icilin Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

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

Soluble ICAM-1 Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Soluble ICAM-1 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Icatibant Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Icatibant metabolite from the curated HMDB Metabolites of Enzymes dataset.

(5Z,8Z,11Z,14Z,17Z)-Icosapentaenoyl-CoA Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the (5Z,8Z,11Z,14Z,17Z)-Icosapentaenoyl-CoA metabolite from the curated HMDB Metabolites of Enzymes dataset.

ichthyosis Gene Set

From HPO Gene-Disease Associations

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

congenital nonbullous ichthyosiform erythroderma Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital nonbullous ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital ichthyosiform erythroderma Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital bullous ichthyosiform erythroderma Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital bullous ichthyosiform erythroderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ichthyosiform Erythroderma, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Ichthyosis, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Ichthyosis Vulgaris Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Ichthyosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Beta-catenin-interacting ICAT Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Beta-catenin-interacting ICAT protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ICln Gene Set

From InterPro Predicted Protein Domain Annotations

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

Integrin binding protein, ICAP-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Integrin binding protein, ICAP-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, ICE, catalytic subunit p20, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, ICE, catalytic subunit p20, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Islet cell autoantigen 1/Ica1-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Islet cell autoantigen 1/Ica1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Islet cell autoantigen Ica1, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Islet cell autoantigen Ica1, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C14, ICE, catalytic subunit p20 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C14, ICE, catalytic subunit p20 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ICP0-binding domain of Ubiquitin-specific protease 7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ICP0-binding domain of Ubiquitin-specific protease 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ICK Gene Set

From KEA Substrates of Kinases

substrates of the kinase ICK from the curated KEA Substrates of Kinases dataset.

ICSBP Gene Set

From MotifMap Predicted Transcription Factor Targets

target genes of the ICSBP transcription factor predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.

ICAM3 Gene Set

From MSigDB Cancer Gene Co-expression Modules

co-expressed genes for ICAM3 from the MSigDB Cancer Gene Co-expression Modules dataset.

ichthyosis, cyclic, with epidermolytic hyperkeratosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, cyclic, with epidermolytic hyperkeratosis phenotype from the curated OMIM Gene-Disease Associations dataset.

hystrix-like ichthyosis with deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the hystrix-like ichthyosis with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis vulgaris Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis vulgaris phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis prematurity syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis prematurity syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, autosomal recessive 4b (harlequin) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, autosomal recessive 4b (harlequin) phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis with confetti Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis with confetti phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, autosomal recessive 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, autosomal recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis bullosa of siemens Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis bullosa of siemens phenotype from the curated OMIM Gene-Disease Associations dataset.

keratitis-ichthyosis-deafness syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratitis-ichthyosis-deafness syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

vohwinkel syndrome with ichthyosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the vohwinkel syndrome with ichthyosis phenotype from the curated OMIM Gene-Disease Associations dataset.

ICMT Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICMT from the Pathway Commons Protein-Protein Interactions dataset.

ICOS Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICOS from the Pathway Commons Protein-Protein Interactions dataset.

ICA1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICA1 from the Pathway Commons Protein-Protein Interactions dataset.

ICK Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICK from the Pathway Commons Protein-Protein Interactions dataset.

ICOSLG Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICOSLG from the Pathway Commons Protein-Protein Interactions dataset.

ICAM4 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICAM4 from the Pathway Commons Protein-Protein Interactions dataset.

ICAM5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICAM5 from the Pathway Commons Protein-Protein Interactions dataset.

ICAM2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICAM2 from the Pathway Commons Protein-Protein Interactions dataset.

ICAM1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICAM1 from the Pathway Commons Protein-Protein Interactions dataset.

ICAM3 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICAM3 from the Pathway Commons Protein-Protein Interactions dataset.

ICT1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ICT1 from the Pathway Commons Protein-Protein Interactions dataset.

ic50 Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term ic50 in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

ICK Gene Set

From PhosphoSitePlus Substrates of Kinases

substrates of the kinase ICK from the curated PhosphoSitePlus Substrates of Kinases dataset.

Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) pathway from the Reactome Pathways dataset.

p12-ichikawa cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue p12-ichikawa cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; edema Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

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

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

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

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance 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.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1; albuminuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 1 and type 2 muscle fiber minicore regions Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 and type 2 muscle fiber minicore regions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

type 1 fibers relatively smaller than type 2 fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 fibers relatively smaller than type 2 fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

P-type ATPase, subfamily IIA, PMR1-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, PMR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

P-type ATPase, subfamily IIA, SERCA-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, SERCA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ephrin receptor type-A /type-B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ephrin receptor type-A /type-B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter, type 1/type 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter, type 1/type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ocular albinism, type i, nettleship-falls type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ocular albinism, type i, nettleship-falls type phenotype from the curated OMIM Gene-Disease Associations dataset.

regulation of ck1/cdk5 by type 1 glutamate receptors Gene Set

From Biocarta Pathways

proteins participating in the regulation of ck1/cdk5 by type 1 glutamate receptors pathway from the Biocarta Pathways dataset.

Bartter syndrome, type 3, with hypocalciuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pachyonychia congenita, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pachyonychia congenita, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohypoparathyroidism type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohypoparathyroidism type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Achondrogenesis type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Achondrogenesis type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA, mut(-) TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA, mut(-) TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohypoaldosteronism, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohypoaldosteronism, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib-polydactyly syndrome, Majewski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ISOVALERIC ACIDEMIA, TYPE I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ISOVALERIC ACIDEMIA, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher's disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Czech dysplasia metatarsal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Czech dysplasia metatarsal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitamin d hydroxylation-deficient rickets, type 1b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitamin d hydroxylation-deficient rickets, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperammonemia, type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperammonemia, type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PROPERDIN DEFICIENCY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Telangiectasia, hereditary hemorrhagic, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Telangiectasia, hereditary hemorrhagic, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive cutis laxa type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive cutis laxa type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic, Claes-Jensen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sialidosis type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sialidosis type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 8 deficiency type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WALDNER TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IVF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital generalized lipodystrophy type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type IXa1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, turner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal chondrodysplasia, miura type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal chondrodysplasia, miura type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Duane syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metaphyseal chondrodysplasia, Jansen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metaphyseal chondrodysplasia, Jansen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, congenital generalized, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Beta-thalassemia, dominant inclusion body type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia, Kozlowski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia, Kozlowski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary hemorrhagic telangiectasia type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary hemorrhagic telangiectasia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metachromatic leukodystrophy, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metachromatic leukodystrophy, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Porokeratosis 8, disseminated superficial actinic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Porokeratosis 8, disseminated superficial actinic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia with joint dislocations, GPAPP type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondrodysplasia with joint dislocations, GPAPP type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corticosterone methyloxidase type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corticosterone methyloxidase type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atelosteogenesis type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atelosteogenesis type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atelosteogenesis type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atelosteogenesis type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atelosteogenesis type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atelosteogenesis type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLCOBALAMIN DEFICIENCY, cblG TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLCOBALAMIN DEFICIENCY, cblG TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa simplex, Koebner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa simplex, Koebner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methylmalonic aciduria cblA type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methylmalonic aciduria cblA type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachydactyly type A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachydactyly type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Citrullinemia type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Citrullinemia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary hyperoxaluria, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary hyperoxaluria, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitamin D-dependent rickets, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitamin D-dependent rickets, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen deficiency, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, Missouri type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, Missouri type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Isolated growth hormone deficiency type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type II, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome, type 4b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, juvenile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial visceral amyloidosis, Ostertag type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune lymphoproliferative syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA, mut(0) TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA, mut(0) TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia, kimberley type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia, kimberley type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen activator inhibitor type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohypoaldosteronism type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohypoaldosteronism type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitamin D-dependent rickets, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitamin D-dependent rickets, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, raymond type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY sex reversal, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY sex reversal, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurofibromatosis, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurofibromatosis, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurofibromatosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic ataxia, type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemochromatosis type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemochromatosis type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemochromatosis type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemochromatosis type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency with hyper IgM type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency with hyper IgM type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency with hyper IgM type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency with hyper IgM type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency with hyper IgM type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency with hyper IgM type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency with hyper IgM type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency with hyper IgM type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tyrosinemia type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tyrosinemia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tyrosinemia type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tyrosinemia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome progeroid type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-Methylglutaconic aciduria type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-Methylglutaconic aciduria type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Larsen syndrome, dominant type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital secretory diarrhea, chloride type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachydactyly type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachydactyly type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trichorhinophalangeal dysplasia type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trichorhinophalangeal dysplasia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corticosterone methyloxidase type 2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corticosterone methyloxidase type 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type X Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Citrullinemia type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Citrullinemia type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thanatophoric dysplasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thanatophoric dysplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Popliteal pterygium syndrome lethal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Multiple pterygium syndrome Escobar type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schwartz Jampel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachydactyly type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachydactyly type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PROPERDIN DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary lymphedema type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary lymphedema type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis autosomal dominant type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis autosomal dominant type 1 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.

Spherocytosis type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spherocytosis type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spherocytosis type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spherocytosis type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrocallosal syndrome, Schinzel type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-Methylglutaconic aciduria type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-Methylglutaconic aciduria type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndactyly type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndactyly type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary hyperoxaluria, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary hyperoxaluria, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia Charlevoix-Saguenay type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia Charlevoix-Saguenay type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome, type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rhizomelic chondrodysplasia punctata type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rhizomelic chondrodysplasia punctata type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 7B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acromesomelic dysplasia Maroteaux type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acromesomelic dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachydactyly type E2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachydactyly type E2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndactyly type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndactyly type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal myopathy Markesbery-Griggs type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2k Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ocular albinism, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ocular albinism, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukocyte adhesion deficiency type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria type V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypokalemic periodic paralysis, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypokalemic periodic paralysis, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic Atrophy Type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucopolysaccharidosis type VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucopolysaccharidosis type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndactyly type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndactyly type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUCOPOLYSACCHARIDOSIS, TYPE VI, INTERMEDIATE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, INTERMEDIATE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple exostoses type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Postaxial polydactyly type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Postaxial polydactyly type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1v Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 5B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Posterior polar cataract type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Posterior polar cataract type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carbohydrate-deficient glycoprotein syndrome type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbohydrate-deficient glycoprotein syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHEMOGLOBINEMIA, TYPE I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHEMOGLOBINEMIA, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spherocytosis type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spherocytosis type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephalic osteodysplastic primordial dwarfism type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephalic osteodysplastic primordial dwarfism type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Methemoglobinemia type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methemoglobinemia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglandular autoimmune syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglandular autoimmune syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pachyonychia congenita type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pachyonychia congenita type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndactyly Cenani Lenz type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndactyly Cenani Lenz type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemochromatosis type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemochromatosis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemochromatosis type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemochromatosis type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary angioedema type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary angioedema type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal arthrogryposis type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohypoaldosteronism type 1 autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohypoaldosteronism type 1 autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HYPERLIPOPROTEINEMIA, TYPE ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HYPERLIPOPROTEINEMIA, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cockayne syndrome type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cockayne syndrome type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY sex reversal, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY sex reversal, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Butyrylcholinesterase deficiency, fluoride-resistant, japanese type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Butyrylcholinesterase deficiency, fluoride-resistant, japanese type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY sex reversal, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY sex reversal, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial amyloid polyneuropathy, Iowa type