Name

GAD High Level Gene-Disease Associations Dataset

From Genetic Association Database

gene-disease associations curated from genetic association studies

CTD Gene-Disease Associations Dataset

From Comparative Toxicogenomics Database

disease-gene interactions curated from literature

DISEASES Curated Gene-Disease Assocation Evidence Scores Dataset

From DISEASES

disease gene evidence scores by manual literature curation

DISEASES Experimental Gene-Disease Assocation Evidence Scores Dataset

From DISEASES

disease gene evidence scores by integrating experimental data (GWAS)

DISEASES Text-mining Gene-Disease Assocation Evidence Scores Dataset

From DISEASES

gene-disease co-occurrence scores from text-mining biomedical abstracts

GAD Gene-Disease Associations Dataset

From Genetic Association Database

gene-disease associations curated from genetic association studies

GWASdb SNP-Disease Associations Dataset

From GWASdb

SNP-disease association p-values curated from published GWAS

HPO Gene-Disease Associations Dataset

From Human Phenotype Ontology

phenotype-causing gene mutations of human phenotypes from disease knowledgebases

OMIM Gene-Disease Associations Dataset

From Online Mendelian Inheritance in Man

disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications

PhosphoSitePlus Phosphosite-Disease Associations Dataset

From PhosphoSitePlus

disease-phosphosite associations curated from literature

SERPINB9 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 9

This gene encodes a member of the serine protease inhibitor family which are also known as serpins. The encoded protein belongs to a subfamily of intracellular serpins. This protein inhibits the activity of the effector molecule granzyme B. Overexpression of this protein may prevent cytotoxic T-lymphocytes from eliminating certain tumor cells. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Mar 2012]

SERPINB8 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 8

The superfamily of high molecular weight serine proteinase inhibitors (serpins) regulate a diverse set of intracellular and extracellular processes such as complement activation, fibrinolysis, coagulation, cellular differentiation, tumor suppression, apoptosis, and cell migration. Serpins are characterized by well-conserved a tertiary structure that consists of 3 beta sheets and 8 or 9 alpha helices (Huber and Carrell, 1989 [PubMed 2690952]). A critical portion of the molecule, the reactive center loop connects beta sheets A and C. Protease inhibitor-8 (PI8; SERPINB8) is a member of the ov-serpin subfamily, which, relative to the archetypal serpin PI1 (MIM 107400), is characterized by a high degree of homology to chicken ovalbumin, lack of N- and C-terminal extensions, absence of a signal peptide, and a serine rather than an asparagine residue at the penultimate position (summary by Bartuski et al., 1997 [PubMed 9268635]).[supplied by OMIM, Jan 2010]

SERPINB1 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 1

The protein encoded by this gene is a member of the serpin family of proteinase inhibitors. Members of this family maintain homeostasis by neutralizing overexpressed proteinase activity through their function as suicide substrates. This protein inhibits the neutrophil-derived proteinases neutrophil elastase, cathepsin G, and proteinase-3 and thus protects tissues from damage at inflammatory sites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

SERPINB3 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 3

SERPINB2 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 2

SERPINB5 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 5

SERPINB4 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 4

SERPINB7 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 7

This gene encodes a member of a family of proteins which function as protease inhibitors. Expression of this gene is upregulated in IgA nephropathy and mutations have been found to cause palmoplantar keratoderma, Nagashima type. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

SERPINB6 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 6

The protein encoded by this gene is a member of the serpin (serine proteinase inhibitor) superfamily, and ovalbumin(ov)-serpin subfamily. It was originally discovered as a placental thrombin inhibitor. The mouse homolog was found to be expressed in the hair cells of the inner ear. Mutations in this gene are associated with nonsyndromic progressive hearing loss, suggesting that this serpin plays an important role in the inner ear in the protection against leakage of lysosomal content during stress, and that loss of this protection results in cell death and sensorineural hearing loss. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]

SERF2 Gene

small EDRK-rich factor 2

SERPINB8P1 Gene

serpin peptidase inhibitor, clade B8 (ovalbumin) pseudogene 1

SERPINH1P1 Gene

serpin peptidase inhibitor, clade H1, pseudogene 1

SERPINI1 Gene

serpin peptidase inhibitor, clade I (neuroserpin), member 1

This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]

SERPINI2 Gene

serpin peptidase inhibitor, clade I (pancpin), member 2

The gene encodes a member of a family of proteins that acts as inhibitors of serine proteases. These proteins function in the regulation of a variety of physiological processes, including coagulation, fibrinolysis, development, malignancy, and inflammation. Expression of the encoded protein may be downregulated during pancreatic carcinogenesis. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013]

SERPINA2 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 2 (gene/pseudogene)

This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. The encoded intracellular glycoprotein is localized at the endoplasmic reticulum. This gene is a polymorphic pseudogene, with the non-functional allele being predominant in some populations. Some individuals, as represented by the reference genome allele, contain a 2kb coding region deletion and a start code mutation. [provided by RefSeq, Feb 2014]

SERPINA3 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3

The protein encoded by this gene is a plasma protease inhibitor and member of the serine protease inhibitor class. Polymorphisms in this protein appear to be tissue specific and influence protease targeting. Variations in this protein's sequence have been implicated in Alzheimer's disease, and deficiency of this protein has been associated with liver disease. Mutations have been identified in patients with Parkinson disease and chronic obstructive pulmonary disease. [provided by RefSeq, Jul 2008]

SERPINA4 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 4

SERPINA5 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5

The protein encoded by this gene is a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. This gene is one in a cluster of serpin genes located on the q arm of chromosome 14. This family member is a glycoprotein that can inhibit several serine proteases, including protein C and various plasminogen activators and kallikreins, and it thus plays diverse roles in hemostasis and thrombosis in multiple organs. [provided by RefSeq, Aug 2012]

SERPINA6 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6

This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008]

SERPINA9 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 9

SERP2 Gene

stress-associated endoplasmic reticulum protein family member 2

SERINC5 Gene

serine incorporator 5

SERINC4 Gene

serine incorporator 4

SERINC1 Gene

serine incorporator 1

SERINC3 Gene

serine incorporator 3

SERINC2 Gene

serine incorporator 2

SERPINB11 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 11 (gene/pseudogene)

SERPINB10 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 10

The superfamily of high molecular weight serine proteinase inhibitors (serpins) regulate a diverse set of intracellular and extracellular processes such as complement activation, fibrinolysis, coagulation, cellular differentiation, tumor suppression, apoptosis, and cell migration. Serpins are characterized by a well-conserved tertiary structure that consists of 3 beta sheets and 8 or 9 alpha helices (Huber and Carrell, 1989 [PubMed 2690952]). A critical portion of the molecule, the reactive center loop connects beta sheets A and C. Protease inhibitor-10 (PI10; SERPINB10) is a member of the ov-serpin subfamily, which, relative to the archetypal serpin PI1 (MIM 107400), is characterized by a high degree of homology to chicken ovalbumin, lack of N- and C-terminal extensions, absence of a signal peptide, and a serine rather than an asparagine residue at the penultimate position (summary by Bartuski et al., 1997 [PubMed 9268635]).[supplied by OMIM, Jan 2010]

SERPINB13 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 13

SERPINB12 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 12

SERBP1P1 Gene

SERPINE1 mRNA binding protein 1 pseudogene 1

SERBP1P3 Gene

SERPINE1 mRNA binding protein 1 pseudogene 3

SERBP1P2 Gene

SERPINE1 mRNA binding protein 1 pseudogene 2

SERBP1P5 Gene

SERPINE1 mRNA binding protein 1 pseudogene 5

SERBP1P4 Gene

SERPINE1 mRNA binding protein 1 pseudogene 4

SERBP1P6 Gene

SERPINE1 mRNA binding protein 1 pseudogene 6

SERPINA7P1 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7 pseudogene 1

SERPIND1 Gene

serpin peptidase inhibitor, clade D (heparin cofactor), member 1

The product encoded by this gene is a serine proteinase inhibitor which rapidly inhibits thrombin in the presence of dermatan sulfate or heparin. The gene contains five exons and four introns. This protein shares homology with antithrombin III and other members of the alpha 1-antitrypsin superfamily. Mutations in this gene are associated with heparin cofactor II deficiency. [provided by RefSeq, Jul 2008]

SERPINB9P1 Gene

serpin peptidase inhibitor, clade B (ovalbumin), member 9, pseudogene 1

SERPINC1 Gene

serpin peptidase inhibitor, clade C (antithrombin), member 1

The protein encoded by this gene is a plasma protease inhibitor and a member of the serpin superfamily. This protein inhibits thrombin as well as other activated serine proteases of the coagulation system, and it regulates the blood coagulation cascade. The protein includes two functional domains: the heparin binding-domain at the N-terminus of the mature protein, and the reactive site domain at the C-terminus. The inhibitory activity is enhanced by the presence of heparin. More than 120 mutations have been identified for this gene, many of which are known to cause antithrombin-III deficiency. [provided by RefSeq, Jul 2009]

SERHL2 Gene

serine hydrolase-like 2

SERTM1 Gene

serine-rich and transmembrane domain containing 1

SERPINA13P Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 13, pseudogene

SERPINF1 Gene

serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1

The protein encoded by this gene is a member of the serpin family, although it does not display the serine protease inhibitory activity shown by many of the other serpin family members. The encoded protein is secreted and strongly inhibits angiogenesis. In addition, this protein is a neurotrophic factor involved in neuronal differentiation in retinoblastoma cells.[provided by RefSeq, Mar 2011]

SERPINF2 Gene

serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2

This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

SERF1A Gene

small EDRK-rich factor 1A (telomeric)

This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The duplication region includes both a telomeric and a centromeric copy of this gene. Deletions of this gene, the telomeric copy, often accompany deletions of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients, and so it is thought that this gene may be a modifier of the SMA phenotype. The function of this protein is not known; however, it bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. [provided by RefSeq, Jul 2008]

SERF1B Gene

small EDRK-rich factor 1B (centromeric)

This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008]

SERF2-C15ORF63 Gene

SERF2-C15orf63 readthrough

This locus represents naturally occurring read-through transcription between the neighboring small EDRK-rich factor 2 (SERF2) and chromosome 15 open reading frame 63 (C15orf63) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD) based on the use of the supported SERF2 start codon, and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]

SERPINE4P Gene

serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 4 pseudogene

SERPINE1 Gene

serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1

This gene encodes a member of the serine proteinase inhibitor (serpin) superfamily. This member is the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), and hence is an inhibitor of fibrinolysis. Defects in this gene are the cause of plasminogen activator inhibitor-1 deficiency (PAI-1 deficiency), and high concentrations of the gene product are associated with thrombophilia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

SERPINE2 Gene

serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2

This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. Thrombin, urokinase, plasmin and trypsin are among the proteases that this family member can inhibit. This gene is a susceptibility gene for chronic obstructive pulmonary disease and for emphysema. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

SERPINE3 Gene

serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 3

SERPINA12 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12

SERPINA10 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10

The protein encoded by this gene belongs to the serpin family. It is predominantly expressed in the liver and secreted in plasma. It inhibits the activity of coagulation factors Xa and XIa in the presence of protein Z, calcium and phospholipid. Mutations in this gene are associated with venous thrombosis. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, May 2010]

SERPINA11 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 11

SERP1 Gene

stress-associated endoplasmic reticulum protein 1

SERPINH1 Gene

serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)

This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The encoded protein is localized to the endoplasmic reticulum and plays a role in collagen biosynthesis as a collagen-specific molecular chaperone. Autoantibodies to the encoded protein have been found in patients with rheumatoid arthritis. Expression of this gene may be a marker for cancer, and nucleotide polymorphisms in this gene may be associated with preterm birth caused by preterm premature rupture of membranes. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, May 2011]

SERGEF Gene

secretion regulating guanine nucleotide exchange factor

SERF1AP1 Gene

small EDRK-rich factor 1A (telomeric) pseudogene 1

SERTAD1 Gene

SERTA domain containing 1

SERTAD2 Gene

SERTA domain containing 2

SERTAD3 Gene

SERTA domain containing 3

The protein encoded by this gene was identified in a yeast two-hybrid assay employing the second subunit of human replication protein A as bait. It is localized to the nucleus and its expression is significantly higher in cancer cell lines compared to normal cell lines. This protein has also been shown to be a strong transcriptional co-activator. Alternative splicing has been observed at this locus and two variants, both encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]

SERTAD4 Gene

SERTA domain containing 4

SERHL Gene

serine hydrolase-like (pseudogene)

SERBP1 Gene

SERPINE1 mRNA binding protein 1

SERPINA15P Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 15, pseudogene

SERPING1 Gene

serpin peptidase inhibitor, clade G (C1 inhibitor), member 1

This gene encodes a highly glycosylated plasma protein involved in the regulation of the complement cascade. Its protein inhibits activated C1r and C1s of the first complement component and thus regulates complement activation. Deficiency of this protein is associated with hereditary angioneurotic oedema (HANE). Alternative splicing results in multiple transcript variants encoding the same isoform. [provided by RefSeq, Jul 2008]

SERPINA1 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1

The protein encoded by this gene is secreted and is a serine protease inhibitor whose targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, and plasminogen activator. Defects in this gene can cause emphysema or liver disease. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

SERPINA7 Gene

serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7

There are three proteins including thyroxine-binding globulin (TBG), transthyretin and albumin responsible for carrying the thyroid hormones thyroxine (T4) and 3,5,3'-triiodothyronine (T3) in the bloodstream. This gene encodes the major thyroid hormone transport protein, TBG, in serum. It belongs to the serpin family in genomics, but the protein has no inhibitory function like many other members of the serpin family. Mutations in this gene result in TGB deficiency, which has been classified as partial deficiency, complete deficiency, and excess, based on the level of serum TBG. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined.[provided by RefSeq, Jun 2012]

SERAC1 Gene

serine active site containing 1

The protein encoded by this gene is a phosphatidylglycerol remodeling protein found at the interface of mitochondria and endoplasmic reticula, where it mediates phospholipid exchange. The encoded protein plays a major role in mitochondrial function and intracellular cholesterol trafficking. Defects in this gene are a cause of 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (MEGDEL). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012]

SERTAD4-AS1 Gene

SERTAD4 antisense RNA 1

CHDS4 Gene

Coronary heart disease, susceptibility to, 4

CHDS3 Gene

Coronary heart disease, susceptibility to, 3

CHDS2 Gene

Coronary heart disease, susceptibility to, 2

CHDS1 Gene

Coronary heart disease, susceptibility to, 1

CHDS9 Gene

Coronary heart disease, suscpetibility to, 9

CHDS8 Gene

Coronary heart disease, susceptibility to, 8

HRTRT1 Gene

Heart rate QTL 1

HAND2 Gene

heart and neural crest derivatives expressed 2

The protein encoded by this gene belongs to the basic helix-loop-helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, this transcription factor plays an important role in limb and branchial arch development. [provided by RefSeq, Jul 2008]

PFHB2 Gene

Progressive familial heart block, type II

HEG1 Gene

heart development protein with EGF-like domains 1

HBN1 Gene

Progressive familial heart block, type I, locus 1

HAND1 Gene

heart and neural crest derivatives expressed 1

The protein encoded by this gene belongs to the basic helix-loop-helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, it has been suggested that this transcription factor may be required for early trophoblast differentiation. [provided by RefSeq, Jul 2008]

LBH Gene

limb bud and heart development

FABP3 Gene

fatty acid binding protein 3, muscle and heart

The intracellular fatty acid-binding proteins (FABPs) belongs to a multigene family. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Fatty acid-binding protein 3 gene contains four exons and its function is to arrest growth of mammary epithelial cells. This gene is a candidate tumor suppressor gene for human breast cancer. [provided by RefSeq, Jul 2008]

CHDT3 Gene

Congenital heart defects, multiple types, 3

RDPA Gene

refsum disease, adult, with increased pipecolicacidemia

NPC2 Gene

Niemann-Pick disease, type C2

This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008]

NPC1 Gene

Niemann-Pick disease, type C1

This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009]

CMT2H Gene

Charcot-Marie-Tooth disease, axonal, type 2H

CMT2G Gene

Charcot-Marie-Tooth disease, axonal, type 2G

GRD2 Gene

Graves disease, susceptibility to, 2

GRD1 Gene

Graves disease, susceptiblity to, 1

GRDX Gene

Graves disease, susceptibility to, X-linked

COPD14 Gene

Chronic obstructive pulmonary disease QTL 14

PDDC1 Gene

Parkinson disease 7 domain containing 1

CELIAC8 Gene

Celiac disease, susceptibility to, 8

CELIAC2 Gene

celiac disease 2

CELIAC5 Gene

Celiac disease, susceptibility to, 5

CELIAC6 Gene

Celiac disease, susceptibility to, 6

CELIAC7 Gene

Celiac disease, susceptibility to, 7

AIS4 Gene

autoimmune disease, susceptibility to, 4

COPD3 Gene

Chronic obstructive pulmonary disease QTL 3

COPD2 Gene

Chronic obstructive pulmonary disease QTL 2

COPD1 Gene

Chronic obstructive pulmonary disease QTL 1

COPD6 Gene

Chronic obstructive pulmonary disease QTL 6

COPD5 Gene

Chronic obstructive pulmonary disease QTL 5

COPD4 Gene

Chronic obstructive pulmonary disease QTL 4

COPD8 Gene

Chronic obstructive pulmonary disease QTL 8

PKHD1L1 Gene

polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1

BED Gene

Bornholm eye disease

PKD1P1 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 1

PKD1P2 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 2

PKD1P3 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 3

PKD1P4 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 4

PKD1P5 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 5

PKD1P6 Gene

polycystic kidney disease 1 (autosomal dominant) pseudogene 6

PKD3 Gene

polycystic kidney disease 3 (autosomal dominant)

PKD2 Gene

polycystic kidney disease 2 (autosomal dominant)

This gene encodes a member of the polycystin protein family. The encoded protein is a multi-pass membrane protein that functions as a calcium permeable cation channel, and is involved in calcium transport and calcium signaling in renal epithelial cells. This protein interacts with polycystin 1, and they may be partners in a common signaling cascade involved in tubular morphogenesis. Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2. [provided by RefSeq, Mar 2011]

PKD1 Gene

polycystic kidney disease 1 (autosomal dominant)

This gene encodes a member of the polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described. [provided by RefSeq, Oct 2008]

OED Gene

Oregon eye disease

GBD3 Gene

gallbladder disease 3

CMTDIA Gene

Charcot-Marie-Tooth disease, dominant intermediate 2

PDB6 Gene

Paget disease of bone 6

PDB4 Gene

Paget disease of bone 4

PDB5 Gene

Paget disease of bone 5

PDB1 Gene

Paget disease of bone 1

IBD9 Gene

inflammatory bowel disease 9

IBD8 Gene

inflammatory bowel disease 8

IBD3 Gene

inflammatory bowel disease 3

IBD2 Gene

inflammatory bowel disease 2

IBD5 Gene

inflammatory bowel disease 5

IBD4 Gene

inflammatory bowel disease 4

IBD7 Gene

inflammatory bowel disease 7

IBD6 Gene

inflammatory bowel disease 6

COPD17 Gene

Chronic obstructive pulmonary disease QTL 17

GBD2 Gene

gallbladder disease 2

PAOD1 Gene

Peripheral arterial occlusive disease 1

COPD7 Gene

Chronic obstructive pulmonary disease QTL 7

COPD9 Gene

Chronic obstructive pulmonary disease QTL 9

DDD3 Gene

Dowling-Degos disease 3

NAFLD2 Gene

Fatty liver disease, nonalcoholic, susceptibility to, 2

NAFLD1 Gene

Fatty liver disease 1, susceptiblity to

EPM2A Gene

epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)

This gene encodes a dual-specificity phosphatase that associates with polyribosomes. The encoded protein may be involved in the regulation of glycogen metabolism. Mutations in this gene have been associated with myoclonic epilepsy of Lafora. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

PKDTS Gene

polycystic kidney disease, infantile severe, with tuberous sclerosis

AITD2 Gene

Autoimmune thyroid disease, susceptibility to, 2

AITD1 Gene

Autoimmune thyroid disease, susceptibility to, 1

AITD4 Gene

Autoimmune thyroid disease, susceptibility to, 4

KWE Gene

keratolytic winter erythema (Oudtshoorn skin disease)

LOC613206 Gene

myeloproliferative disease associated tumor antigen 5

RMD1 Gene

rippling muscle disease 1

AD10 Gene

Alzheimer disease-10

AD11 Gene

Alzheimer disease-11

AD12 Gene

Alzheimer disease 12

AD13 Gene

Alzheimer disease-13

AD14 Gene

Alzheimer disease 14

AD16 Gene

Alzheimer disease 16

AD17 Gene

Alzheimer disease 17

PKD1L1 Gene

polycystic kidney disease 1 like 1

This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]

PKD1L2 Gene

polycystic kidney disease 1-like 2 (gene/pseudogene)

This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores. This gene appears to be a polymorphic pseudogene in humans, where some individuals contain a non-functional allele. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

PKD1L3 Gene

polycystic kidney disease 1-like 3

This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores.[provided by RefSeq, Apr 2009]

HDPA Gene

Hodgkin disease, susceptibility, pseudoautosomal

AD6 Gene

Alzheimer disease 6

AD7 Gene

Alzheimer disease 7

AD5 Gene

Alzheimer disease 5

AD8 Gene

Alzheimer disease 8

AD9 Gene

Alzheimer disease 9

PARK16 Gene

Parkinson disease 16 (susceptibility)

PARK10 Gene

Parkinson disease 10 (susceptibility)

PARK12 Gene

Parkinson disease 12 (susceptibility)

HSCR9 Gene

Hirschsprung disease, susceptibility to, 9

HSCR8 Gene

Hirschsprung disease modifier 2

HSCR5 Gene

Hirschsprung disease, susceptibility to, 5

The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. Patients are diagnosed with the short-segment form (S-HSCR, approximately 80% of cases) when the aganglionic segment does not extend beyond the upper sigmoid, and with the long-segment form (L-HSCR) when aganglionosis extends proximal to the sigmoid. Total colonic aganglionosis and total intestinal HSCR also occur (Amiel et al., 2008 [PubMed 17965226]). Isolated HSCR appears to be of complex nonmendelian inheritance with low sex-dependent penetrance and variable expression according to the length of the aganglionic segment, suggestive of the involvement of one or more genes with low penetrance (Amiel et al., 2008 [PubMed 17965226]). For a general description and a discussion of genetic heterogeneity of Hirschsprung disease (HSCR), see MIM 142623.[supplied by OMIM, Feb 2011]

HSCR7 Gene

Hirschsprung disease, short-segment, 3

HSCR6 Gene

Hirschsprung disease, short-segment, 2

IBD27 Gene

Inflammatory bowel disease-27

IBD20 Gene

Inflammatory bowel disease-20

IBD21 Gene

Inflammatory bowel disease-21

IBD22 Gene

Inflammatory bowel disease-22

IBD23 Gene

Inflammatory bowel disease-23

IBD24 Gene

Inflammatory bowel disease-24

IBD25 Gene

Inflammatory bowel disease-25

IBD26 Gene

Inflammatory bowel disease-26

CCAL1 Gene

chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)

PARK3 Gene

Parkinson disease 3 (autosomal dominant, Lewy body)

CELIAC9 Gene

Celiac disease, susceptibility to, 9

CTD Gene

Coats disease

AD15 Gene

Alzheimer disease-15

COPD13 Gene

Chronic obstructive pulmonary disease QTL 13

COPD12 Gene

Chronic obstructive pulmonary disease QTL 12

COPD11 Gene

Chronic obstructive pulmonary disease QTL 11

COPD10 Gene

Chronic obstructive pulmonary disease QTL 10

COPD16 Gene

Chronic obstructive pulmonary disease QTL 16

COPD15 Gene

Chronic obstructive pulmonary disease QTL 15

COPD19 Gene

Chronic obstructive pulmonary disease QTL 19

COPD18 Gene

Chronic obstructive pulmonary disease QTL 18

MYMY1 Gene

moyamoya disease 1

MYMY3 Gene

moyamoya disease 3

MYMY4 Gene

Moyamoya disease 4

COPD Gene

Pulmonary disease, chronic obstructive, severe early-onset

IBD11 Gene

Inflammatory bowel disease 11

IBD12 Gene

Inflammatory bowel disease 12

IBD15 Gene

Inflammatory bowel disease-15

IBD16 Gene

Inflammatory bowel disease-16

IBD19 Gene

Inflammatory bowel disease 19

IBD18 Gene

Inflammatory bowel disease-18

NDP Gene

Norrie disease (pseudoglioma)

This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy. [provided by RefSeq, Feb 2009]

PKHD1 Gene

polycystic kidney and hepatic disease 1 (autosomal recessive)

The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008]

PKD2L2 Gene

polycystic kidney disease 2-like 2

PKD2L1 Gene

polycystic kidney disease 2-like 1

This gene encodes a member of the polycystin protein family. The encoded protein contains multiple transmembrane domains, and cytoplasmic N- and C-termini. The protein may be an integral membrane protein involved in cell-cell/matrix interactions. This protein functions as a calcium-regulated nonselective cation channel. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

COPD28 Gene

Chronic obstructive pulmonary disease QTL 28

COPD29 Gene

Chronic obstructive pulmonary disease QTL 29

COPD22 Gene

Chronic obstructive pulmonary disease QTL 22

COPD23 Gene

Chronic obstructive pulmonary disease QTL 23

COPD20 Gene

Chronic obstructive pulmonary disease QTL 20

COPD21 Gene

Chronic obstructive pulmonary disease QTL 21

COPD26 Gene

Chronic obstructive pulmonary disease QTL 26

COPD27 Gene

Chronic obstructive pulmonary disease QTL 27

COPD24 Gene

Chronic obstructive pulmonary disease QTL 24

COPD25 Gene

Chronic obstructive pulmonary disease QTL 25

CELIAC12 Gene

Celiac disease, susceptibility to, 12

CELIAC13 Gene

Celiac disease, susceptibility to, 13

CELIAC10 Gene

Celiac disease, susceptibility to, 10

CELIAC11 Gene

Celiac disease, susceptibility to, 11

HMGN2P31 Gene

high mobility group nucleosomal binding domain 2 pseudogene 31

HMGB3P5 Gene

high mobility group box 3 pseudogene 5

HMGN2P19 Gene

high mobility group nucleosomal binding domain 2 pseudogene 19

HMGN2P18 Gene

high mobility group nucleosomal binding domain 2 pseudogene 18

HMGN2P12 Gene

high mobility group nucleosomal binding domain 2 pseudogene 12

HMGN2P11 Gene

high mobility group nucleosomal binding domain 2 pseudogene 11

HMGN2P10 Gene

high mobility group nucleosomal binding domain 2 pseudogene10

HMGN2P17 Gene

high mobility group nucleosomal binding domain 2 pseudogene 17

HMGN2P16 Gene

high mobility group nucleosomal binding domain 2 pseudogene 16

HMGN2P15 Gene

high mobility group nucleosomal binding domain 2 pseudogene 15

HMGN2P14 Gene

high mobility group nucleosomal binding domain 2 pseudogene14

FCER1G Gene

Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide

The high affinity IgE receptor is a key molecule involved in allergic reactions. It is a tetramer composed of 1 alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. [provided by RefSeq, Jul 2008]

FCER1A Gene

Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide

The immunoglobulin epsilon receptor (IgE receptor) is the initiator of the allergic response. When two or more high-affinity IgE receptors are brought together by allergen-bound IgE molecules, mediators such as histamine that are responsible for allergy symptoms are released. This receptor is comprised of an alpha subunit, a beta subunit, and two gamma subunits. The protein encoded by this gene represents the alpha subunit. [provided by RefSeq, Aug 2011]

HMGN1P9 Gene

high mobility group nucleosome binding domain 1 pseudogene

HMGN1P4 Gene

high mobility group nucleosome binding domain 1 pseudogene 4

HMGN1P5 Gene

high mobility group nucleosome binding domain 1 pseudogene 5

HMGN1P6 Gene

high mobility group nucleosome binding domain 1 pseudogene 6

HMGN1P7 Gene

high mobility group nucleosome binding domain 1 pseudogene 7

HMGN1P1 Gene

high mobility group nucleosome binding domain 1 pseudogene 1

HMGN1P2 Gene

high mobility group nucleosome binding domain 1 pseudogene 2

LOC100129956 Gene

high mobility group nucleosomal binding domain 2 pseudogene

HMGB3 Gene

high mobility group box 3

This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

HMGB4 Gene

high mobility group box 4

HMGN2P13 Gene

high mobility group nucleosomal binding domain 2 pseudogene 13

HMGB1P12 Gene

high mobility group box 1 pseudogene 12

HMGB1P10 Gene

high mobility group box 1 pseudogene 10

HMGB1P16 Gene

high mobility group box 1 pseudogene 16

HMGB1P17 Gene

high mobility group box 1 pseudogene 17

HMGB1P36 Gene

high mobility group box 1 pseudogene 36

HMGB3P22 Gene

high mobility group box 3 pseudogene 22

MYP18 Gene

myopia 18 (high grade, autosomal recessive)

This locus was identified by linkage in one consanguineous Chinese family to lie between D14S984 and D14S999. [provided by RefSeq, Feb 2010]

MYP11 Gene

myopia 11 (high grade, autosomal dominant)

HMGN1P8 Gene

high mobility group nucleosome binding domain 1 pseudogene 8

HMGN1P3 Gene

high mobility group nucleosome binding domain 1 pseudogene 3

HMGB1P1 Gene

high mobility group box 1 pseudogene 1

This gene may represent an evolving retropseudogene of the high-mobility group box 1 gene, which has multiple pseudogenes. This gene has an intact open reading frame, where the length of encoded protein is conserved, compared to the high-mobility group box 1 protein. However, due to the lack of conclusive evidence for specific transcription at this location, this locus is currently represented as a pseudogene. [provided by RefSeq, Jan 2010]

HMGB1P3 Gene

high mobility group box 1 pseudogene 3

HMGB1P4 Gene

high mobility group box 1 pseudogene 4

HMGB1P5 Gene

high mobility group box 1 pseudogene 5

HMGN1P16 Gene

high mobility group nucleosome binding domain 1 pseudogene 16

HMGN1P17 Gene

high mobility group nucleosome binding domain 1 pseudogene 17

HMGN1P13 Gene

high mobility group nucleosome binding domain 1 pseudogene 13

HMGN1P10 Gene

high mobility group nucleosome binding domain 1 pseudogene 10

HMGN1P11 Gene

high mobility group nucleosome binding domain 1 pseudogene 11

HDLCQ6 Gene

High density lipoprotein cholesterol level QTL 6

HDLCQ1 Gene

high density lipoprotein cholesterol level QTL 1

HMGN1P33 Gene

high mobility group nucleosome binding domain 1 pseudogene 33

HMGN1P34 Gene

high mobility group nucleosome binding domain 1 pseudogene 34

HMGB3P32 Gene

high mobility group box 3 pseudogene 32

HMGB3P30 Gene

high mobility group box 3 pseudogene 30

HMGB3P31 Gene

high mobility group box 3 pseudogene 31

HMGN2P33 Gene

high mobility group nucleosomal binding domain 2 pseudogene 33

HMGN2P32 Gene

high mobility group nucleosomal binding domain 2 pseudogene 32

HMGN2P35 Gene

high mobility group nucleosomal binding domain 2 pseudogene 35

HMGN2P34 Gene

high mobility group nucleosomal binding domain 2 pseudogene 34

HMGN2P37 Gene

high mobility group nucleosomal binding domain 2 pseudogene 37

HMGN2P36 Gene

high mobility group nucleosomal binding domain 2 pseudogene 36

HMGN2P39 Gene

high mobility group nucleosomal binding domain 2 pseudogene 39

HMGN2P38 Gene

high mobility group nucleosomal binding domain 2 pseudogene 38

HMGB1P27 Gene

high mobility group box 1 pseudogene 27

HMGB1P24 Gene

high mobility group box 1 pseudogene 24

HMGB1P22 Gene

high mobility group box 1 pseudogene 22

HMGB1P29 Gene

high mobility group box 1 pseudogene 29

HDLBP Gene

high density lipoprotein binding protein

The protein encoded by this gene binds high density lipoprotein (HDL) and may function to regulate excess cholesterol levels in cells. The encoded protein also binds RNA and can induce heterochromatin formation. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

NTSR1 Gene

neurotensin receptor 1 (high affinity)

Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secretion. [provided by RefSeq, Jul 2008]

HMGB1P18 Gene

high mobility group box 1 pseudogene 18

HMGB1P19 Gene

high mobility group box 1 pseudogene 19

HMGB1P11 Gene

high mobility group box 1 pseudogene 11

HMGB1P14 Gene

high mobility group box 1 pseudogene 14

HMGB1P15 Gene

high mobility group box 1 pseudogene 15

HMGB2 Gene

high mobility group box 2

This gene encodes a member of the non-histone chromosomal high mobility group protein family. The proteins of this family are chromatin-associated and ubiquitously distributed in the nucleus of higher eukaryotic cells. In vitro studies have demonstrated that this protein is able to efficiently bend DNA and form DNA circles. These studies suggest a role in facilitating cooperative interactions between cis-acting proteins by promoting DNA flexibility. This protein was also reported to be involved in the final ligation step in DNA end-joining processes of DNA double-strand breaks repair and V(D)J recombination. [provided by RefSeq, Jul 2008]

HMGB1 Gene

high mobility group box 1

HMGN3P1 Gene

high mobility group nucleosomal binding domain 3 pseudogene 1

HMGB1P45 Gene

high mobility group box 1 pseudogene 45

HMGA2 Gene

high mobility group AT-hook 2

This gene encodes a protein that belongs to the non-histone chromosomal high mobility group (HMG) protein family. HMG proteins function as architectural factors and are essential components of the enhancesome. This protein contains structural DNA-binding domains and may act as a transcriptional regulating factor. Identification of the deletion, amplification, and rearrangement of this gene that are associated with myxoid liposarcoma suggests a role in adipogenesis and mesenchymal differentiation. A gene knock out study of the mouse counterpart demonstrated that this gene is involved in diet-induced obesity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

HMGB1P41 Gene

high mobility group box 1 pseudogene 41

HMGB1P40 Gene

high mobility group box 1 pseudogene 40

HMGB1P44 Gene

high mobility group box 1 pseudogene 44

HMGB1P47 Gene

high mobility group box 1 pseudogene 47

HMGB1P49 Gene

high mobility group box 1 pseudogene 49

HMGB1P48 Gene

high mobility group box 1 pseudogene 48

HMGN1P23 Gene

high mobility group nucleosome binding domain 1 pseudogene 23

HMGN1P22 Gene

high mobility group nucleosome binding domain 1 pseudogene 22

HMGN1P21 Gene

high mobility group nucleosome binding domain 1 pseudogene 21

HMGN1P27 Gene

high mobility group nucleosome binding domain 1 pseudogene 27

HMGN1P26 Gene

high mobility group nucleosome binding domain 1 pseudogene 26

HMGN1P25 Gene

high mobility group nucleosome binding domain 1 pseudogene 25

HMGN1P24 Gene

high mobility group nucleosome binding domain 1 pseudogene 24

HMGN1P29 Gene

high mobility group nucleosome binding domain 1 pseudogene 29

HMGN1P28 Gene

high mobility group nucleosome binding domain 1 pseudogene 28

HMGB3P2 Gene

high mobility group box 3 pseudogene 2

HMGB3P3 Gene

high mobility group box 3 pseudogene 3

HMGB3P1 Gene

high mobility group box 3 pseudogene 1

HMGB3P6 Gene

high mobility group box 3 pseudogene 6

HMGB3P7 Gene

high mobility group box 3 pseudogene 7

HMGB3P4 Gene

high mobility group box 3 pseudogene 4

HMGB3P8 Gene

high mobility group box 3 pseudogene 8

HMGB3P9 Gene

high mobility group box 3 pseudogene 9

HMG20A Gene

high mobility group 20A

HMG20B Gene

high mobility group 20B

HMGA1P4 Gene

high mobility group AT-hook 1 pseudogene 4

HMGA1P6 Gene

high mobility group AT-hook 1 pseudogene 6

HMGB1P34 Gene

high mobility group box 1 pseudogene 34

HMGB1P37 Gene

high mobility group box 1 pseudogene 37

HMGB1P30 Gene

high mobility group box 1 pseudogene 30

HMGB1P38 Gene

high mobility group box 1 pseudogene 38

HMGB1P39 Gene

high mobility group box 1 pseudogene 39

HMGN1P35 Gene

high mobility group nucleosome binding domain 1 pseudogene 35

HMGB1P35 Gene

high mobility group box 1 pseudogene 35

HMGB1P31 Gene

high mobility group box 1 pseudogene 31

HMGB1P32 Gene

high mobility group box 1 pseudogene 32

HMGN5 Gene

high mobility group nucleosome binding domain 5

This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009]

HMGN4 Gene

high mobility group nucleosomal binding domain 4

The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]

HMGN3 Gene

high mobility group nucleosomal binding domain 3

Thyroid hormone receptors are hormone-dependent transcription factors that regulate expression of a variety of specific target genes. The protein encoded by this gene binds thyroid hormone receptor beta, but only in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]

HMGN2 Gene

high mobility group nucleosomal binding domain 2

The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014]

HMGN1 Gene

high mobility group nucleosome binding domain 1

The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011]

HMGA1P8 Gene

high mobility group AT-hook 1 pseudogene 8 (functional)

HMGA1P5 Gene

high mobility group AT-hook 1 pseudogene 5

HMGA1P7 Gene

high mobility group AT-hook 1 pseudogene 7

HMGA1P1 Gene

high mobility group AT-hook 1 pseudogene 1

HMGA1P3 Gene

high mobility group AT-hook 1 pseudogene 3

HMGA1P2 Gene

high mobility group AT-hook 1 pseudogene 2

HMGB1P33 Gene

high mobility group box 1 pseudogene 33

MYP12 Gene

myopia 12 (high grade, autosomal dominant)

HMGA1 Gene

high mobility group AT-hook 1

This gene encodes a non-histone protein involved in many cellular processes, including regulation of inducible gene transcription, integration of retroviruses into chromosomes, and the metastatic progression of cancer cells. The encoded protein preferentially binds to the minor groove of A+T-rich regions in double-stranded DNA. It has little secondary structure in solution but assumes distinct conformations when bound to substrates such as DNA or other proteins. The encoded protein is frequently acetylated and is found in the nucleus. At least seven transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

HMGN2P30 Gene

high mobility group nucleosomal binding domain 2 pseudogene 30

HMGN2P26 Gene

high mobility group nucleosomal binding domain 2 pseudogene 26

HMGN2P27 Gene

high mobility group nucleosomal binding domain 2 pseudogene 27

HMGN2P22 Gene

high mobility group nucleosomal binding domain 2 pseudogene 22

HMGN2P23 Gene

high mobility group nucleosomal binding domain 2 pseudogene 23

HMGN2P20 Gene

high mobility group nucleosomal binding domain 2 pseudogene 20

HMGN2P21 Gene

high mobility group nucleosomal binding domain 2 pseudogene 21

GPIHBP1 Gene

glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1

This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) family. This protein plays a major role in transporting lipoprotein lipase (LPL) from the subendothelial spaces to the capillary lumen. Mutations in this gene are the cause of hyperlipoproteinemia, type 1D. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]

HMGN2P7 Gene

high mobility group nucleosomal binding domain 2 pseudogene 7

HMGN2P6 Gene

high mobility group nucleosomal binding domain 2 pseudogene 6

HMGN2P5 Gene

high mobility group nucleosomal binding domain 2 pseudogene 5

HMGN2P3 Gene

high mobility group nucleosomal binding domain 2 pseudogene 3

HMGN2P2 Gene

high mobility group nucleosomal binding domain 2 pseudogene 2

HMGN2P1 Gene

high mobility group nucleosomal binding domain 2 pseudogene 1

HMGN2P9 Gene

high mobility group nucleosomal binding domain 2 pseudogene 9

HMGB1P26 Gene

high mobility group box 1 pseudogene 26

HMGB1P23 Gene

high mobility group box 1 pseudogene 23

HMGB1P28 Gene

high mobility group box 1 pseudogene 28

HMGB1P8 Gene

high mobility group box 1 pseudogene 8

HMGB1P9 Gene

high mobility group box 1 pseudogene 9

FCGR1C Gene

Fc fragment of IgG, high affinity Ic, receptor (CD64), pseudogene

The gene represents one of three related immunoglobulin gamma Fc receptor genes located on chromosome 1. This family member lacks the transmembrane and coiled-coiled domains found in other family members and is thought to be a pseudogene of Fc-gamma-receptor 1A. [provided by RefSeq, Apr 2009]

FCGR1B Gene

Fc fragment of IgG, high affinity Ib, receptor (CD64)

Three distinct, but closely related classes of receptors that bind the Fc portion of IgG have been identified (Fcgamma RI, II and III). The FcgammaRI family consists of three closely related genes termed A, B, and C. This gene encodes the low affinity FcgammaRIB receptor that may play an important role in humoral immune response. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]

FCGR1A Gene

Fc fragment of IgG, high affinity Ia, receptor (CD64)

This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1. [provided by RefSeq, Jul 2008]

HMGN1P14 Gene

high mobility group nucleosome binding domain 1 pseudogene 14

HMGN1P15 Gene

high mobility group nucleosome binding domain 1 pseudogene 15

HMGN1P19 Gene

high mobility group nucleosome binding domain 1 pseudogene 19

HMGB1P25 Gene

high mobility group box 1 pseudogene 25

HMGB1P21 Gene

high mobility group box 1 pseudogene 21

HMGB1P20 Gene

high mobility group box 1 pseudogene 20

HTL Gene

high L-leucine transport

HMGB1P43 Gene

high mobility group box 1 pseudogene 43

HMGB1P42 Gene

high mobility group box 1 pseudogene 42

HMGB1P46 Gene

high mobility group box 1 pseudogene 46

HMGB2P1 Gene

high mobility group box 2 pseudogene 1

HMGN1P18 Gene

high mobility group nucleosome binding domain 1 pseudogene 18

HMGB1P13 Gene

high mobility group box 1 pseudogene 13

HMGB3P25 Gene

high mobility group box 3 pseudogene 25

HMGB3P24 Gene

high mobility group box 3 pseudogene 24

HMGB3P27 Gene

high mobility group box 3 pseudogene 27

HMGB3P26 Gene

high mobility group box 3 pseudogene 26

HMGB3P20 Gene

high mobility group box 3 pseudogene 20

HMGN2P28 Gene

high mobility group nucleosomal binding domain 2 pseudogene 28

HMGN2P29 Gene

high mobility group nucleosomal binding domain 2 pseudogene 29

HMGN2P25 Gene

high mobility group nucleosomal binding domain 2 pseudogene 25

HMGN2P24 Gene

high mobility group nucleosomal binding domain 2 pseudogene 24

HMGN1P30 Gene

high mobility group nucleosome binding domain 1 pseudogene 30

HMGN1P31 Gene

high mobility group nucleosome binding domain 1 pseudogene 31

HMGN1P32 Gene

high mobility group nucleosome binding domain 1 pseudogene 32

HMGN1P36 Gene

high mobility group nucleosome binding domain 1 pseudogene 36

HMGN1P37 Gene

high mobility group nucleosome binding domain 1 pseudogene 37

HMGN1P38 Gene

high mobility group nucleosome binding domain 1 pseudogene 38

TOX Gene

thymocyte selection-associated high mobility group box

The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]

HMGB1P6 Gene

high mobility group box 1 pseudogene 6

HMGB1P7 Gene

high mobility group box 1 pseudogene 7

HMGN2P44 Gene

high mobility group nucleosomal binding domain 2 pseudogene 44

HMGN2P45 Gene

high mobility group nucleosomal binding domain 2 pseudogene 45

HMGN2P46 Gene

high mobility group nucleosomal binding domain 2 pseudogene 46

HMGN2P40 Gene

high mobility group nucleosomal binding domain 2 pseudogene 40

HMGN2P41 Gene

high mobility group nucleosomal binding domain 2 pseudogene 41

HMGN2P42 Gene

high mobility group nucleosomal binding domain 2 pseudogene 42

HMGN2P43 Gene

high mobility group nucleosomal binding domain 2 pseudogene 43

TOX4 Gene

TOX high mobility group box family member 4

TOX3 Gene

TOX high mobility group box family member 3

The protein encoded by this gene contains an HMG-box, indicating that it may be involved in bending and unwinding of DNA and alteration of chromatin structure. The C-terminus of the encoded protein is glutamine-rich due to CAG repeats in the coding sequence. A minor allele of this gene has been implicated in an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2009]

TOX2 Gene

TOX high mobility group box family member 2

FCAMR Gene

Fc receptor, IgA, IgM, high affinity

HDLCQ4 Gene

High density lipoprotein cholesterol level QTL 4

HDLCQ5 Gene

High density lipoprotein cholesterol level QTL 5

HDLCQ2 Gene

High density lipoprotein cholesterol level QTL on chromosome 8

HMGN1P20 Gene

high mobility group nucleosome binding domain 1 pseudogene 20

HMGB3P14 Gene

high mobility group box 3 pseudogene 14

HMGB3P15 Gene

high mobility group box 3 pseudogene 15

HMGB3P16 Gene

high mobility group box 3 pseudogene 16

HMGB3P17 Gene

high mobility group box 3 pseudogene 17

HMGB3P10 Gene

high mobility group box 3 pseudogene 10

HMGB3P11 Gene

high mobility group box 3 pseudogene 11

HMGB3P12 Gene

high mobility group box 3 pseudogene 12

HMGB3P13 Gene

high mobility group box 3 pseudogene 13

HMGB3P18 Gene

high mobility group box 3 pseudogene 18

HMGB3P19 Gene

high mobility group box 3 pseudogene 19

MYP2 Gene

myopia 2 (high grade, autosomal dominant)

MYP3 Gene

myopia 3 (high grade, autosomal dominant)

MYP4 Gene

myopia 4 (high grade, autosomal dominant)

MYP5 Gene

myopia 5 (high grade, autosomal dominant)

HDLC3 Gene

High density lipoprotein cholesterol, low serum, 3

HMGB3P29 Gene

high mobility group box 3 pseudogene 29

HMGB3P28 Gene

high mobility group box 3 pseudogene 28

HMGB3P21 Gene

high mobility group box 3 pseudogene 21

HMGB3P23 Gene

high mobility group box 3 pseudogene 23

HMGN2P4 Gene

high mobility group nucleosomal binding domain 2 pseudogene 4

HMGN2P8 Gene

high mobility group nucleosomal binding domain 2 pseudogene 8

LOC100421281 Gene

high density lipoprotein binding protein pseudogene

SLC1A6 Gene

solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6

SLC1A1 Gene

solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1

This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]

SLC1A2 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 2

This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Mutations in and decreased expression of this protein are associated with amyotrophic lateral sclerosis. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Sep 2010]

SLC1A3 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 3

This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]

TOX4P1 Gene

TOX high mobility group box family member 4 pseudogene 1

CCHE1 Gene

cervical carcinoma high-expressed lncRNA 1

high coronary heart disease risk particularly affects ser Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high coronary heart disease risk particularly affects ser in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; graft vs host disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation 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.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; 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.

apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; hypertension Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia 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.

coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications 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.

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation Gene Set

From GAD Gene-Disease Associations

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

apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism 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.

communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; recurrence Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dilatation, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis 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.

coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction 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.

coronary disease; coronary heart disease; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia 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.

arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary artery vasospasm; coronary vasospasm; recurrence Gene Set

From GAD Gene-Disease Associations

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

particularly Gene Set

From GeneRIF Biological Term Annotations

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

affects Gene Set

From GeneRIF Biological Term Annotations

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

coronary artery disease risk Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease-reduced risk Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease risk factors Gene Set

From GAD Gene-Disease Associations

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

high tnf levels is not a risk factor for venous thromboem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high tnf levels is not a risk factor for venous thromboem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuroblastoma (high-risk) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuroblastoma (high-risk) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Neuroblastoma (high-risk) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Neuroblastoma (high-risk) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

coronary heart disease and serum very low density lipopro Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and serum very low density lipopro in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

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

high plasma concentrations of high density lipoprotein ch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma concentrations of high density lipoprotein ch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced risk of restenosis after coronary stenting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced risk of restenosis after coronary stenting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune 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; 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; hypertension; rheumatoid arthritis 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.

acute coronary syndrome; coronary disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary atherosclerosis Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary restenosis; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary thrombosis; hemorrhage Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; coronary artery disease; rupture, spontaneous Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary stenosis; Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; coronary artery disease; Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary restenosis; hypertension Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary stenosis; graft occlusion, vascular Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

acute coronary syndrome; cardiovascular diseases; coronary artery disease; Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary stenosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; calcinosis; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis; Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary stenosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis; graft occlusion, vascular Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary thrombosis Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary stenosis Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis; hyperplasia Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease in non-type 1 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease in non-type 1 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease among japanese. Gene Set

From GAD Gene-Disease Associations

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

type 2 diabetes ; coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; heart disease, ischemic; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; atherosclerosis, coronary; hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; atherosclerosis, coronary; hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease in younger individuals. Gene Set

From GAD Gene-Disease Associations

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

coronary atherosclerotic heart disease in chinese Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease; lipids; lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease; lipids; lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; heart failure; hypertension; kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; heart failure; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; coronary heart disease; lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; coronary heart disease; lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; heart diseases; recurrence Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; heart failure; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease and plasma lipid levels. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and plasma lipid levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease. Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease in non-insulin-dependent diabetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease in non-insulin-dependent diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary heart disease. Gene Set

From GAD Gene-Disease Associations

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

coronary heart disease, transplant associated Gene Set

From GAD Gene-Disease Associations

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

Coronary heart disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary heart disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

{coronary heart disease, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary heart disease, susceptibility to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary heart disease, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart valve diseases; rheumatic heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart valve diseases; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-output congestive heart failure Gene Set

From HPO Gene-Disease Associations

genes associated with the high-output congestive heart failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cardiovascular disease risk Gene Set

From GAD Gene-Disease Associations

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

triglycerides; insulin; cardiovascular disease risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; insulin; cardiovascular disease risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease risk factors Gene Set

From GAD Gene-Disease Associations

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

Cardiovascular disease risk factors Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cardiovascular disease risk factors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

high serum ige concentrations Gene Set

From GAD Gene-Disease Associations

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

elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high nonceruloplasmin-bound serum copper Gene Set

From HPO Gene-Disease Associations

genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high maternal serum alpha-fetoprotein Gene Set

From HPO Gene-Disease Associations

genes associated with the high maternal serum alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{high density lipoprotein cholesterol, low serum, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {high density lipoprotein cholesterol, low serum, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

[gamma-glutamyltransferase, familial high serum] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; disease susceptibility; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease/coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary restenosis; coronary stenosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary restenosis; coronary stenosis; diabetes complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary restenosis; coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary occlusion; coronary stenosis; diabetes complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary occlusion; coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; acute coronary syndrome Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

coronary restenosis; coronary stenosis; graft occlusion, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary restenosis; coronary stenosis; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; coronary stenosis; diabetes complications; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; coronary stenosis; diabetes complications; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary restenosis; coronary stenosis Gene Set

From GAD Gene-Disease Associations

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

blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular risk Gene Set

From GAD Gene-Disease Associations

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

increased chromosome aberrations and higher lung cancer risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infectious risk and outcome in surgical intensive care patients Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infectious risk and outcome in surgical intensive care patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastric carcinoma risk Gene Set

From GAD Gene-Disease Associations

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

reduced risk of osteoporotic fractures case control study Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced risk of osteoporotic fractures case control study in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer risk Gene Set

From GAD Gene-Disease Associations

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

financial and psychological risk attitudes Gene Set

From GAD Gene-Disease Associations

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

decreased risk of insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased risk of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes; reduced prostate cancer risk Gene Set

From GAD Gene-Disease Associations

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

neoplasms; decreased cancer risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; decreased cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary and sporadic prostate cancer risk. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary and sporadic prostate cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

circulating protein c levels and thrombotic risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease circulating protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased fracture risk Gene Set

From GAD Gene-Disease Associations

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

lung cancer risk Gene Set

From GAD Gene-Disease Associations

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

anthropometric and metabolic traits, relative to cardiovascular risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anthropometric and metabolic traits, relative to cardiovascular risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma protein c levels and thrombotic risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased cutaneous melanoma risk Gene Set

From GAD Gene-Disease Associations

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

bone density; fracture risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

wegener's granulomatosis- reduced risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wegener's granulomatosis- reduced risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma folate vitamin b12 homocyst(e)ine and colorectal cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

risk factors and tumor characteristics Gene Set

From GAD Gene-Disease Associations

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

liver cancer risk in hcv antibody-positive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver cancer risk in hcv antibody-positive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular risk; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular risk; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular risk factors Gene Set

From GAD Gene-Disease Associations

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

diet lifestyle and risk of colon cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diet lifestyle and risk of colon cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombotic risk factors Gene Set

From GAD Gene-Disease Associations

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

risk-taking behavior in a gambling task Gene Set

From GAD Gene-Disease Associations

genes associated with the disease risk-taking behavior in a gambling task in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden cardiac arrest risk Gene Set

From GAD Gene-Disease Associations

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

decreased risk of cerebrovascular mortality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased risk of cerebrovascular mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

endometrial cancer risk. Gene Set

From GAD Gene-Disease Associations

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

decreased lung cancer risk Gene Set

From GAD Gene-Disease Associations

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

increased lung cancer risk Gene Set

From GAD Gene-Disease Associations

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

risk of cervical dysplasia Gene Set

From GAD Gene-Disease Associations

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

reduced risk of lung cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced risk of lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine risk Gene Set

From GAD Gene-Disease Associations

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

financial risk taking Gene Set

From GAD Gene-Disease Associations

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

increasing risk and a poor prognosis of renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increasing risk and a poor prognosis of renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer risk and prenatal viability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast cancer risk and prenatal viability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

risk Gene Set

From GeneRIF Biological Term Annotations

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

Suicide risk Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Suicide risk phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hypertension risk in short sleep duration Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

{macular degeneration, age-related, 14, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{colonic adenoma recurrence, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {colonic adenoma recurrence, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{macular degeneration, age-related, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, cerebral, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{gastric cancer risk after h. pylori infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {gastric cancer risk after h. pylori infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disease progression Gene Set

From GAD Gene-Disease Associations

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

crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

addison disease; graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

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

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis; crohn disease; crohn's disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

2,3-bis(palmitoyloxy)-2-propyl-N-palmitoyl-cysteinyl-seryl-seryl-asparaginyl-alanine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 2,3-bis(palmitoyloxy)-2-propyl-N-palmitoyl-cysteinyl-seryl-seryl-asparaginyl-alanine from the curated CTD Gene-Chemical Interactions dataset.

serum folate and serum total homocysteine Gene Set

From GAD Gene-Disease Associations

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

Premature coronary artery disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coronary artery disease, autosomal dominant 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coronary Artery Disease Gene Set

From CTD Gene-Disease Associations

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

Coronary Artery Disease, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Coronary Disease Gene Set

From CTD Gene-Disease Associations

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

Coronary Artery Disease, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Coronary Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Coronary Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Coronary Artery Disease Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Coronary Artery Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

coronary artery disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease coronary artery disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

coronary artery disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

coronary artery disease; death, sudden; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; aortic stiffness Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

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

coronary disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; graft occlusion, vascular Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; coronary disease Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

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

angiographic coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

early coronary disease. Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

calcinosis; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; lipoproteins; fluvastatin, clinical events with; treatment with fluvastatin, response to Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; lipoproteins; fluvastatin, clinical events with; treatment with fluvastatin, response to in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; obesity Gene Set

From GAD Gene-Disease Associations

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

coronary disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; diabetes mellitus, type 1; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

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

coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

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

coronary disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; coronary disease; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; erectile dysfunction Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary artery disease; Gene Set

From GAD Gene-Disease Associations

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

apoplexy; coronary artery disease; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; lupus erythematosus, systemic Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease; colorectal cancer; ace activity; coronary atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease; colorectal cancer; ace activity; coronary atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene Set

From GAD Gene-Disease Associations

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

coronary disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

chlamydophila infections; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary disease; diabetes mellitus, type 2; diabetic nephropathies; Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

coronary artery disease; kidney failure; uremia Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; thrombosis Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary artery disease; diabetes complications; graft occlusion, vascular; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes complications; graft occlusion, vascular; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; inflammation; postoperative complications Gene Set

From GAD Gene-Disease Associations

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

coronary disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; triglycerides; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; triglycerides; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes complications Gene Set

From GAD Gene-Disease Associations

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

angina, unstable; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease and myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

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

metabolic syndrome and electrocardiographic coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; kidney diseases Gene Set

From GAD Gene-Disease Associations

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

hypercholesterolemia coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hypertension Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; gout; metabolic syndrome x; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; gout; metabolic syndrome x; myocardial infarction 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.

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.

coronary artery disease; insulin resistance; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary artery disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; coronary disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; hypertension; fabry's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; hypertension; fabry's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes complications; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; syndrome Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; inflammation; periodontitis Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease. plasma lipoproteins. and longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease. plasma lipoproteins. and longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; diabetes complications; hypercholesterolemia; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; diabetes complications; hypercholesterolemia; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

calcinosis; coronary artery disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperparathyroidism, primary Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes mellitus, type 1; diabetic nephropathies Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hyperhomocysteinemia; postoperative complications Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease and plasma soluble thrombomodulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease and plasma soluble thrombomodulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; coronary artery disease; hypertension Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

coronary disease; graft occlusion, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; nitric oxide Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; dyslipidemias; Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

brain ischemia; coronary disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; cytomegalovirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary artery disease; cytomegalovirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes, type 2 Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; plaque, atherosclerotic Gene Set

From GAD Gene-Disease Associations

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

aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes, type 2; lipoproteins; longevity Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease, occlusive Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease. Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes mellitus; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; migraine disorders Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; recurrence Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; restenosis Gene Set

From GAD Gene-Disease Associations

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

coronary disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

coronary disease; hypertension Gene Set

From GAD Gene-Disease Associations

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

coronary disease; inflammation Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hemochromatosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hypertension; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

premature coronary artery disease. Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cardiovascular diseases; coronary disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

calcinosis; coronary artery disease; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

calcinosis; carotid artery diseases; coronary artery disease; diabetes mellitus, type 2; Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; diabetes mellitus, type 2; periodontitis Gene Set

From GAD Gene-Disease Associations

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

coronary disease; diabetes complications; hemochromatosis; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; diabetes complications; hemochromatosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; kidney neoplasms Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; stroke Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

atrial fibrillation; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; hyperlipoproteinemia type ii; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; hyperlipoproteinemia type ii; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; diabetic angiopathies; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; diabetic angiopathies; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary artery disease; kidney failure, chronic; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary artery disease; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; intraoperative complications; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

chlamydophila infections; coronary disease Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cigarette smoking. coronary artery disease. and diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cigarette smoking. coronary artery disease. and diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; inflammation Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary artery disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; p-selectin Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary disease; factor xii deficiency; hypercholesterolemia; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; factor xii deficiency; hypercholesterolemia; hypertension 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.

brain ischemia; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

premature coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary disease Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; Gene Set

From GAD Gene-Disease Associations

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

coronary disease Gene Set

From GAD Gene-Disease Associations

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

atrial fibrillation; coronary disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; coronary disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Coronary artery disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary artery disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Coronary artery disease or ischemic stroke Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary artery disease or ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Coronary artery disease or large artery stroke Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Coronary artery disease or large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

coronary artery disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease coronary artery disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

coronary artery disease Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the coronary artery disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

coronary artery disease Gene Set

From HPO Gene-Disease Associations

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

premature coronary artery disease Gene Set

From HPO Gene-Disease Associations

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

Coronary Artery Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Coronary Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Junctional protein associated with coronary artery disease Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Junctional protein associated with coronary artery disease protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{coronary artery disease, autosomal dominant, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease, autosomal dominant, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease, autosomal dominant, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease, autosomal dominant, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease in familial hypercholesterolemia, protection against} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease in familial hypercholesterolemia, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.

{coronary artery disease, resistance to} Gene Set

From OMIM Gene-Disease Associations

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

{coronary artery disease} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {coronary artery disease} phenotype from the curated OMIM Gene-Disease Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

heart valve disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart conduction disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

chronic pulmonary heart disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease chronic pulmonary heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart conduction disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease heart conduction disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

heart disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease heart disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

chronic pulmonary heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

heart valve disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute pulmonary heart disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

heart disease Gene Set