| Name |
|---|
LOC728613 Geneprogrammed cell death 6 pseudogene |
ANKDD1A Geneankyrin repeat and death domain containing 1A Predicted to be involved in signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
ANKDD1B Geneankyrin repeat and death domain containing 1B Predicted to be involved in signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
CDIP1 Genecell death-inducing p53 target 1 Predicted to enable zinc ion binding activity. Acts upstream of or within intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator. Located in cytoplasmic side of late endosome membrane; cytoplasmic side of lysosomal membrane; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DAPL1 Genedeath associated protein-like 1 Predicted to enable ribosome binding activity; translation initiation factor binding activity; and translation repressor activity. Predicted to be involved in several processes, including cellular response to amino acid starvation; negative regulation of CD8-positive, alpha-beta T cell activation; and negative regulation of metabolic process. Predicted to act upstream of or within cell population proliferation and gene expression. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DAP3P1 Genedeath associated protein 3 pseudogene 1 |
DAP3P2 Genedeath associated protein 3 pseudogene 2 |
CRADD GeneCASP2 and RIPK1 domain containing adaptor with death domain This gene encodes a protein containing a death domain (DD) motif. This protein recruits caspase 2/ICH1 to the cell death signal transduction complex, which includes tumor necrosis factor receptor 1 (TNFR1A) and RIPK1/RIP kinase, and acts in promoting apoptosis. A mutation in this gene was associated with cognitive disability. A related pseudogene is found on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
PDCD1LG2 Geneprogrammed cell death 1 ligand 2 Involved in negative regulation of activated T cell proliferation; negative regulation of interleukin-10 production; and negative regulation of type II interferon production. Predicted to be located in plasma membrane. Predicted to be active in external side of plasma membrane. Biomarker of pulmonary tuberculosis. [provided by Alliance of Genome Resources, Mar 2025] |
LOC286059 Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain pseudogene |
NRADDP Geneneurotrophin receptor associated death domain, pseudogene The neurotrophin receptor alike death domain proteins belong to the death domain superfamily and are involved in mediating apoptosis. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008] |
PIDD1 Genep53-induced death domain protein 1 The protein encoded by this gene contains a leucine-rich repeat and a death domain. This protein has been shown to interact with other death domain proteins, such as Fas (TNFRSF6)-associated via death domain (FADD) and MAP-kinase activating death domain-containing protein (MADD), and thus may function as an adaptor protein in cell death-related signaling processes. The expression of the mouse counterpart of this gene has been found to be positively regulated by the tumor suppressor p53 and to induce cell apoptosis in response to DNA damage, which suggests a role for this gene as an effector of p53-dependent apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010] |
FADD GeneFas (TNFRSF6)-associated via death domain The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development. [provided by RefSeq, Jul 2008] |
ERICD GeneE2F1-regulated inhibitor of cell death (non-protein coding) |
TRADD GeneTNFRSF1A-associated via death domain The protein encoded by this gene is a death domain containing adaptor molecule that interacts with TNFRSF1A/TNFR1 and mediates programmed cell death signaling and NF-kappaB activation. This protein binds adaptor protein TRAF2, reduces the recruitment of inhibitor-of-apoptosis proteins (IAPs) by TRAF2, and thus suppresses TRAF2 mediated apoptosis. This protein can also interact with receptor TNFRSF6/FAS and adaptor protein FADD/MORT1, and is involved in the Fas-induced cell death pathway. [provided by RefSeq, Jul 2008] |
LOC100132609 Geneprogrammed cell death 2 pseudogene |
DAPK3 Genedeath-associated protein kinase 3 Death-associated protein kinase 3 (DAPK3) induces morphological changes in apoptosis when overexpressed in mammalian cells. These results suggest that DAPK3 may play a role in the induction of apoptosis. [provided by RefSeq, Jul 2008] |
DAPK2 Genedeath-associated protein kinase 2 This gene encodes a protein that belongs to the serine/threonine protein kinase family. This protein contains a N-terminal protein kinase domain followed by a conserved calmodulin-binding domain with significant similarity to that of death-associated protein kinase 1 (DAPK1), a positive regulator of programmed cell death. Overexpression of this gene was shown to induce cell apoptosis. It uses multiple polyadenylation sites. [provided by RefSeq, Jul 2008] |
DAPK1 Genedeath-associated protein kinase 1 Death-associated protein kinase 1 is a positive mediator of gamma-interferon induced programmed cell death. DAPK1 encodes a structurally unique 160-kD calmodulin dependent serine-threonine kinase that carries 8 ankyrin repeats and 2 putative P-loop consensus sites. It is a tumor suppressor candidate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013] |
CIDECP Genecell death-inducing DFFA-like effector c pseudogene |
LOC100422426 GeneCASP2 and RIPK1 domain containing adaptor with death domain pseudogene |
LOC105378775 Genecell death regulator Aven-like |
DAP4C Genedeath-associated protein 4C |
BLID GeneBH3-like motif containing, cell death inducer This gene encodes a BH3-like motif containing protein involved in cell death. The encoded protein may induce apoptosis in a caspase-dependent manner. The protein is localized in both the cytoplasm and the mitochondrion. [provided by RefSeq, Aug 2011] |
CIDEC Genecell death-inducing DFFA-like effector c This gene encodes a member of the cell death-inducing DNA fragmentation factor-like effector family. Members of this family play important roles in apoptosis. The encoded protein promotes lipid droplet formation in adipocytes and may mediate adipocyte apoptosis. This gene is regulated by insulin and its expression is positively correlated with insulin sensitivity. Mutations in this gene may contribute to insulin resistant diabetes. A pseudogene of this gene is located on the short arm of chromosome 3. Alternatively spliced transcript variants that encode different isoforms have been observed for this gene. [provided by RefSeq, Dec 2010] |
CIDEA Genecell death-inducing DFFA-like effector a This gene encodes the homolog of the mouse protein Cidea that has been shown to activate apoptosis. This activation of apoptosis is inhibited by the DNA fragmentation factor DFF45 but not by caspase inhibitors. Mice that lack functional Cidea have higher metabolic rates, higher lipolysis in brown adipose tissue and higher core body temperatures when subjected to cold. These mice are also resistant to diet-induced obesity and diabetes. This suggests that in mice this gene product plays a role in thermogenesis and lipolysis. Alternatively spliced transcripts have been identified. [provided by RefSeq, Aug 2010] |
PDCD6 Geneprogrammed cell death 6 This gene encodes a calcium-binding protein belonging to the penta-EF-hand protein family. Calcium binding is important for homodimerization and for conformational changes required for binding to other protein partners. This gene product participates in T cell receptor-, Fas-, and glucocorticoid-induced programmed cell death. In mice deficient for this gene product, however, apoptosis was not blocked suggesting this gene product is functionally redundant. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is also located on the short arm of chromosome 5. [provided by RefSeq, May 2012] |
PDCD7 Geneprogrammed cell death 7 This gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP), which is a component of the minor U12-type spliceosome responsible for catalyzing pre-mRNA splicing of U12-type introns. [provided by RefSeq, Dec 2010] |
PDCD4 Geneprogrammed cell death 4 (neoplastic transformation inhibitor) This gene is a tumor suppressor and encodes a protein that binds to the eukaryotic translation initiation factor 4A1 and inhibits its function by preventing RNA binding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010] |
PDCD5 Geneprogrammed cell death 5 This gene encodes a protein that is upregulated during apoptosis where it translocates rapidly from the cytoplasm to the nucleus. The encoded protein may be an important regulator of K(lysine) acetyltransferase 5 (a protein involved in transcription, DNA damage response and cell cycle control) by inhibiting its proteasome-dependent degradation. Pseudogenes have been identified on chromosomes 5 and 12 [provided by RefSeq, Dec 2010] |
PDCD2 Geneprogrammed cell death 2 This gene encodes a nuclear protein expressed in a variety of tissues. Expression of this gene has been shown to be repressed by B-cell CLL/lymphoma 6 (BCL6), a transcriptional repressor required for lymph node germinal center development, suggesting that BCL6 regulates apoptosis by its effects on this protein. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 9 and 12. [provided by RefSeq, Dec 2010] |
PDCD1 Geneprogrammed cell death 1 Programmed cell death protein 1 (PDCD1) is an immune-inhibitory receptor expressed in activated T cells; it is involved in the regulation of T-cell functions, including those of effector CD8+ T cells. In addition, this protein can also promote the differentiation of CD4+ T cells into T regulatory cells. PDCD1 is expressed in many types of tumors including melanomas, and has demonstrated to play a role in anti-tumor immunity. Moreover, this protein has been shown to be involved in safeguarding against autoimmunity, however, it can also contribute to the inhibition of effective anti-tumor and anti-microbial immunity. [provided by RefSeq, Aug 2020] |
PDCD10 Geneprogrammed cell death 10 This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008] |
PDCD11 Geneprogrammed cell death 11 PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation of 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008] |
PDCD5P1 Geneprogrammed cell death 5 pseudogene 1 |
PDCD5P2 Geneprogrammed cell death 5 pseudogene 2 |
TNFRSF10D Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain, a transmembrane domain, and a truncated cytoplamic death domain. This receptor does not induce apoptosis, and has been shown to play an inhibitory role in TRAIL-induced cell apoptosis. [provided by RefSeq, Jul 2008] |
DIDO1 Genedeath inducer-obliterator 1 Apoptosis, a major form of cell death, is an efficient mechanism for eliminating unwanted cells and is of central importance for development and homeostasis in metazoan animals. In mice, the death inducer-obliterator-1 gene is upregulated by apoptotic signals and encodes a cytoplasmic protein that translocates to the nucleus upon apoptotic signal activation. When overexpressed, the mouse protein induced apoptosis in cell lines growing in vitro. This gene is similar to the mouse gene and therefore is thought to be involved in apoptosis. Alternatively spliced transcripts have been found for this gene, encoding multiple isoforms. [provided by RefSeq, Jul 2008] |
DAD1P1 Genedefender against cell death 1 pseudogene 1 |
LOC100128686 Geneprogrammed cell death 10 pseudogene |
DAXX Genedeath-domain associated protein This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008] |
PDCD2L Geneprogrammed cell death 2-like Predicted to be involved in apoptotic process. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
DEDD Genedeath effector domain containing This gene encodes a protein that contains a death effector domain (DED). DED is a protein-protein interaction domain shared by adaptors, regulators and executors of the programmed cell death pathway. Overexpression of this gene was shown to induce weak apoptosis. Upon stimulation, this protein was found to translocate from cytoplasm to nucleus and colocalize with UBTF, a basal factor required for RNA polymerase I transcription, in the nucleolus. At least three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
MADD GeneMAP-kinase activating death domain Tumor necrosis factor alpha (TNF-alpha) is a signaling molecule that interacts with one of two receptors on cells targeted for apoptosis. The apoptotic signal is transduced inside these cells by cytoplasmic adaptor proteins. The protein encoded by this gene is a death domain-containing adaptor protein that interacts with the death domain of TNF-alpha receptor 1 to activate mitogen-activated protein kinase (MAPK) and propagate the apoptotic signal. It is membrane-bound and expressed at a higher level in neoplastic cells than in normal cells. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
LOC728739 Geneprogrammed cell death 2 pseudogene |
LRRD1 Geneleucine-rich repeats and death domain containing 1 Predicted to be involved in signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
BAD GeneBCL2-associated agonist of cell death The protein encoded by this gene is a member of the BCL-2 family. BCL-2 family members are known to be regulators of programmed cell death. This protein positively regulates cell apoptosis by forming heterodimers with BCL-xL (B-cell lymphoma-extra large) and BCL-2, and reversing their death repressor activity. Proapoptotic activity of this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the regulation of this protein. Alternative splicing of this gene results in two transcript variants which encode the same isoform. [provided by RefSeq, Dec 2019] |
DTHD1 Genedeath domain containing 1 This gene encodes a protein which contains a death domain. Death domain-containing proteins function in signaling pathways and formation of signaling complexes, as well as the apoptosis pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012] |
BID GeneBH3 interacting domain death agonist This gene encodes a death agonist that heterodimerizes with either agonist BAX or antagonist BCL2, and thus regulate apoptosis. The encoded protein is a member of the BCL-2 family of cell death regulators. It is a mediator of mitochondrial damage induced by caspase-8 (CASP8); CASP8 cleaves this encoded protein, and the COOH-terminal part translocates to mitochondria where it triggers cytochrome c release. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Aug 2020] |
DAP Genedeath-associated protein This gene encodes a basic, proline-rich, 15-kD protein. The protein acts as a positive mediator of programmed cell death that is induced by interferon-gamma. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014] |
DEDD2 Genedeath effector domain containing 2 This gene encodes a nuclear-localized protein containing a death effector domain (DED). The encoded protein may regulate the trafficking of caspases and other proteins into the nucleus during death receptor-induced apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012] |
CIDEB Genecell death-inducing DFFA-like effector b Enables identical protein binding activity. Involved in lipid droplet fusion and positive regulation of apoptotic process. Acts upstream of or within apoptotic process. Located in cytosol and perinuclear region of cytoplasm. Is active in lipid droplet. [provided by Alliance of Genome Resources, Mar 2025] |
FAS GeneFas cell surface death receptor The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains a death domain. It has been shown to play a central role in the physiological regulation of programmed cell death, and has been implicated in the pathogenesis of various malignancies and diseases of the immune system. The interaction of this receptor with its ligand allows the formation of a death-inducing signaling complex that includes Fas-associated death domain protein (FADD), caspase 8, and caspase 10. The autoproteolytic processing of the caspases in the complex triggers a downstream caspase cascade, and leads to apoptosis. This receptor has been also shown to activate NF-kappaB, MAPK3/ERK1, and MAPK8/JNK, and is found to be involved in transducing the proliferating signals in normal diploid fibroblast and T cells. Several alternatively spliced transcript variants have been described, some of which are candidates for nonsense-mediated mRNA decay (NMD). The isoforms lacking the transmembrane domain may negatively regulate the apoptosis mediated by the full length isoform. [provided by RefSeq, Mar 2011] |
LOC100131557 Geneprogrammed cell death 2-like pseudogene |
LOC100420576 Genedeath-associated protein kinase 1 pseudogene |
DAD1 Genedefender against cell death 1 DAD1, the defender against apoptotic cell death, was initially identified as a negative regulator of programmed cell death in the temperature sensitive tsBN7 cell line. The DAD1 protein disappeared in temperature-sensitive cells following a shift to the nonpermissive temperature, suggesting that loss of the DAD1 protein triggered apoptosis. DAD1 is believed to be a tightly associated subunit of oligosaccharyltransferase both in the intact membrane and in the purified enzyme, thus reflecting the essential nature of N-linked glycosylation in eukaryotes. [provided by RefSeq, Jul 2008] |
PDCD6IP Geneprogrammed cell death 6 interacting protein This gene encodes a protein that functions within the ESCRT pathway in the abscission stage of cytokinesis, in intralumenal endosomal vesicle formation, and in enveloped virus budding. Studies using mouse cells have shown that overexpression of this protein can block apoptosis. In addition, the product of this gene binds to the product of the PDCD6 gene, a protein required for apoptosis, in a calcium-dependent manner. This gene product also binds to endophilins, proteins that regulate membrane shape during endocytosis. Overexpression of this gene product and endophilins results in cytoplasmic vacuolization, which may be partly responsible for the protection against cell death. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. Related pseudogenes have been identified on chromosome 15. [provided by RefSeq, Jan 2012] |
DAP3 Genedeath associated protein 3 Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein that also participates in apoptotic pathways which are initiated by tumor necrosis factor-alpha, Fas ligand, and gamma interferon. This protein potentially binds ATP/GTP and might be a functional partner of the mitoribosomal protein S27. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Pseudogenes corresponding to this gene are found on chromosomes 1q and 2q. [provided by RefSeq, Dec 2010] |
EDARADD GeneEDAR-associated death domain This gene was identified by its association with ectodermal dysplasia, a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands. The protein encoded by this gene is a death domain-containing protein, and is found to interact with EDAR, a death domain receptor known to be required for the development of hair, teeth and other ectodermal derivatives. This protein and EDAR are coexpressed in epithelial cells during the formation of hair follicles and teeth. Through its interaction with EDAR, this protein acts as an adaptor, and links the receptor to downstream signaling pathways. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
LOC101927197 Genecell death activator CIDE-3-like |
DELE1 GeneDAP3 binding cell death enhancer 1 Enables protein kinase binding activity and protein serine/threonine kinase activator activity. Involved in several processes, including HRI-mediated signaling; positive regulation of mitophagy; and response to iron ion starvation. Located in mitochondrial inner membrane. Is active in cytosol and mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CIDECP1 Genecell death inducing DFFA like effector c pseudogene 1 |
TMDD1 Genetransmembrane and death domain 1 Predicted to be involved in signal transduction. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LCDR Genelysosome cell death regulator |
death in childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Death In Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Death in childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene SetFrom 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. |
death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; heart diseases; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; heart diseases; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; myocardial ischemia; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; diabetes mellitus; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Sudden Unexplained Death In Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden unexplained death in childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
induction of apoptosis through dr3 and dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
Sudden cardiac death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth retardation, developmental delay, coarse facies, and early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sudden infant death syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
death-inducing signaling complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cd95 death-inducing signaling complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cd95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cd95 death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cd95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
trail death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the trail death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Setproteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset. |
Death-inducing signaling complex DISC (type I cells associated), stimulated Gene Setproteins in the Death-inducing signaling complex DISC (type I cells associated), stimulated protein complex from the CORUM Protein Complexes dataset. |
Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Setproteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset. |
Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Death from the curated CTD Gene-Disease Associations dataset. |
Death, Sudden, Cardiac Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Death, Sudden, Cardiac from the curated CTD Gene-Disease Associations dataset. |
Fetal Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Death from the curated CTD Gene-Disease Associations dataset. |
Death, Sudden Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Death, Sudden from the curated CTD Gene-Disease Associations dataset. |
Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome from the curated CTD Gene-Disease Associations dataset. |
Sudden Infant Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sudden Infant Death from the curated CTD Gene-Disease Associations dataset. |
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset. |
Death, Sudden, Cardiac Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Death, Sudden, Cardiac in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
sudden infant death syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sudden infant death syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
myocardial infarct; cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; death, sudden; myocardial infarction Gene SetFrom 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 SetFrom 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; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene SetFrom 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. |
arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sids/sudden infant death syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sids/sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; myocardial infarction; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiac death; cardiac morbidity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac death; cardiac morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; death, sudden, cardiac Gene SetFrom 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. |
myocardial infarction; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo loss; fetal death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; pre-eclampsia; pregnancy complications; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; brain death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; death, sudden, cardiac Gene SetFrom 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. |
cardiac arrhythmias and sudden death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac arrhythmias and sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
staphylococcal infections; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease staphylococcal infections; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; heart diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sudden infant death syndrome (sids) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sudden infant death syndrome (sids) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadaver; cardiovascular diseases; death, sudden, cardiac; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadaver; cardiovascular diseases; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early onset of sudden infant death. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy; heart failure; sudden death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart failure; sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrioventricular block; death, sudden; syncope; torsades de pointes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; death, sudden, cardiac; Gene SetFrom 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. |
long qt syndrome; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; death, sudden, cardiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden, cardiac; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism, inborn errors; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ischemic neuronal cell death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ischemic neuronal cell death 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 SetFrom 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. |
sudden infant death syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term death in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial outer membrane permeabilization involved in programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of retinal cell programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation-induced cell death of t cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of programmed cell death in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
developmental programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of hydrogen peroxide-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of activation-induced cell death of t cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
ectopic germ cell programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ectopic germ cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by symbiont of host programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of activation-induced cell death of t cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of activation-induced cell death of t cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of hydrogen peroxide-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by symbiont of host programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hydrogen peroxide-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hydrogen peroxide-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
induction of programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
retinal cell programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
host programmed cell death induced by symbiont Gene SetFrom GO Biological Process Annotations 2015 genes participating in the host programmed cell death induced by symbiont biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of retinal cell programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
autophagic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation by symbiont of host programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
programmed cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cd95 death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cd95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
death receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
death effector domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
death domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
death receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Aging (time to death) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
sudden cardiac death Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sudden cardiac death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
time of death Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the time of death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sudden death Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sudden death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sudden cardiac death Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden cardiac death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neonatal death Gene SetFrom HPO Gene-Disease Associations genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
death in infancy Gene SetFrom HPO Gene-Disease Associations genes associated with the death in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
time of death Gene SetFrom HPO Gene-Disease Associations genes associated with the time of death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sudden death Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
death in early adulthood Gene SetFrom HPO Gene-Disease Associations genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Brain Death Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Brain Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Death Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Death, Sudden, Cardiac Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Death, Sudden, Cardiac phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fetal Death Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Death, Sudden Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Death, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sudden Infant Death Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sudden Infant Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Death-like domain of Spt6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Death-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Death domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF2428, death-receptor-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF2428, death-receptor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell death regulator Aven Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell death regulator Aven protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Death-associated protein kinase 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-associated protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
BH3-interacting domain death agonist Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the BH3-interacting domain death agonist protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Death effector domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death effector domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Caffeine-induced death protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Caffeine-induced death protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Programmed cell death protein 2, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Programmed cell death protein 2, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sensitivity to induced cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sensitivity to induced cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal induced cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased activation-induced cell death of t cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
premature death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pregnancy-related premature death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal activation-induced cell death of t cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{sudden infant death syndrome, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {sudden infant death syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
sudden infant death with dysgenesis of the testes syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
growth retardation, developmental delay, coarse facies, and early death Gene SetFrom OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset. |
death Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term death in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Cell death signalling via NRAGE, NRIF and NADE Gene Setproteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways dataset. |
Stimulation of the cell death response by PAK-2p34 Gene Setproteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways dataset. |
Death Receptor Signalling Gene Setproteins participating in the Death Receptor Signalling pathway from the Reactome Pathways dataset. |
TRIF-mediated programmed cell death Gene Setproteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways dataset. |
NADE modulates death signalling Gene Setproteins participating in the NADE modulates death signalling pathway from the Reactome Pathways dataset. |
NRIF signals cell death from the nucleus Gene Setproteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways dataset. |
NRAGE signals death through JNK Gene Setproteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways dataset. |
Programmed Cell Death Gene Setproteins participating in the Programmed Cell Death pathway from the Reactome Pathways dataset. |
Sudden Unexplained Death In Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Infant Death Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Infant Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Unexpected Nocturnal Death Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexpected Nocturnal Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Unexplained Infant Death Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Infant Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Infant Death With Dysgenesis Of The Testes Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Infant Death With Dysgenesis Of The Testes Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Death In Infancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Cardiac Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Death In Early Adulthood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Early Adulthood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Risk Of Sudden Cardiac Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Risk Of Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cardiac Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Determination Of Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Determination Of Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neonatal Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Death Anxiety Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death Anxiety in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Embryo Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Brain Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Near Sudden Infant Death Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Near Sudden Infant Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unexplained Sudden Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unexplained Sudden Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Perinatal Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perinatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aborted Sudden Cardiac Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aborted Sudden Cardiac Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Arrhythmic Death Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Arrhythmic Death Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Infant Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infant Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
positive regulation of activated T cell autonomous cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2023 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of hydrogen peroxide-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of hydrogen peroxide-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial outer membrane permeabilization involved in programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2023 genes participating in the activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset. |
autophagic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
programmed cell death in response to reactive oxygen species Gene SetFrom GO Biological Process Annotations 2023 genes participating in the programmed cell death in response to reactive oxygen species biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset. |
death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hydrogen peroxide-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
induction of programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of activated T cell autonomous cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hydrogen peroxide-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hydrogen peroxide-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
CD95 death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the CD95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
death receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
death receptor agonist activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the death receptor agonist activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
death domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
death receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
death effector domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
premature death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased sensitivity to induced cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased sensitivity to induced cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pregnancy-related premature death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal interdigital cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cell death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cell death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased activation-induced cell death of T cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased activation-induced cell death of T cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
sudden unexpected death in epilepsy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sudden unexpected death in epilepsy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Nanoparticle triggered autophagic cell death Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Nanoparticle triggered autophagic cell death pathway from the WikiPathways Pathways 2024 dataset. |
Sudden infant death syndrome SIDS susceptibility pathways Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Sudden infant death syndrome SIDS susceptibility pathways pathway from the WikiPathways Pathways 2024 dataset. |
Caspase activation via Death Receptors in the presence of ligand Gene Setproteins participating in the Caspase activation via Death Receptors in the presence of ligand pathway from the Reactome Pathways 2024 dataset. |
Cell death signalling via NRAGE, NRIF and NADE Gene Setproteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways 2024 dataset. |
Death Receptor Signaling Gene Setproteins participating in the Death Receptor Signaling pathway from the Reactome Pathways 2024 dataset. |
Diseases of programmed cell death Gene Setproteins participating in the Diseases of programmed cell death pathway from the Reactome Pathways 2024 dataset. |
FOXO-mediated transcription of cell death genes Gene Setproteins participating in the FOXO-mediated transcription of cell death genes pathway from the Reactome Pathways 2024 dataset. |
NADE modulates death signalling Gene Setproteins participating in the NADE modulates death signalling pathway from the Reactome Pathways 2024 dataset. |
NRAGE signals death through JNK Gene Setproteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways 2024 dataset. |
NRIF signals cell death from the nucleus Gene Setproteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways 2024 dataset. |
Programmed Cell Death Gene Setproteins participating in the Programmed Cell Death pathway from the Reactome Pathways 2024 dataset. |
Regulation of necroptotic cell death Gene Setproteins participating in the Regulation of necroptotic cell death pathway from the Reactome Pathways 2024 dataset. |
SARS-CoV-1-mediated effects on programmed cell death Gene Setproteins participating in the SARS-CoV-1-mediated effects on programmed cell death pathway from the Reactome Pathways 2024 dataset. |
Stimulation of the cell death response by PAK-2p34 Gene Setproteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways 2024 dataset. |
TLR3-mediated TICAM1-dependent programmed cell death Gene Setproteins participating in the TLR3-mediated TICAM1-dependent programmed cell death pathway from the Reactome Pathways 2024 dataset. |
TP53 Regulates Transcription of Cell Death Genes Gene Setproteins participating in the TP53 Regulates Transcription of Cell Death Genes pathway from the Reactome Pathways 2024 dataset. |
TP53 Regulates Transcription of Death Receptors and Ligands Gene Setproteins participating in the TP53 Regulates Transcription of Death Receptors and Ligands pathway from the Reactome Pathways 2024 dataset. |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain Gene Setproteins participating in the TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain pathway from the Reactome Pathways 2024 dataset. |
TRIF-mediated programmed cell death Gene Setproteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways 2024 dataset. |
positive regulation of activated T cell autonomous cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2025 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset. |
activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2025 genes participating in the activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
pyroptotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the pyroptotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
cytotoxic T cell pyroptotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cytotoxic T cell pyroptotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial outer membrane permeabilization involved in programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
autophagic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
programmed cell death in response to reactive oxygen species Gene SetFrom GO Biological Process Annotations 2025 genes participating in the programmed cell death in response to reactive oxygen species biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset. |
death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
programmed necrotic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
induction of programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of activation-induced cell death of T cells Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of activation-induced cell death of T cells biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of activated T cell autonomous cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of hydrogen peroxide-mediated programmed cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of autophagic cell death Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of death-inducing signaling complex assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
CD95 death-inducing signaling complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the CD95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
death receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
death receptor agonist activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the death receptor agonist activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
death receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
death domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
death effector domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Sudden infant death syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sudden infant death syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
death-inducing signaling complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
CD95 death-inducing signaling complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the CD95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
CD95 death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the CD95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
TRAIL death-inducing signaling complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the TRAIL death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Sudden unexplained death Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SUDDEN INFANT DEATH SYNDR Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SUDDEN INFANT DEATH SYNDR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sudden cardiac death Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Death in early adulthood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in early adulthood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Family history of sudden cardiac death Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Family history of sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neurodegenerative illness progressing to crippling dystonia and death Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodegenerative illness progressing to crippling dystonia and death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neonatal death Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sudden infant death-dysgenesis of the testes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden infant death-dysgenesis of the testes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cardiovascular death or myocardial infarction in response to clopidogrel treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular death or myocardial infarction in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aging (time to death) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parental longevity (mother's age at death) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parental longevity (father's age at death) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (father's age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parental longevity (combined parental age at death) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (combined parental age at death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parental longevity (mother's age at death or mother's attained age) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (mother's age at death or mother's attained age) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PROGRAMMED CELL DEATH 1 LIGAND 1 Gene Setinteracting proteins for the PROGRAMMED CELL DEATH 1 LIGAND 1 drug from theDGIdb Drug Targets 2026 dataset. |
North american indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epileptic encephalopathy, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alternating hemiplegia of childhood Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercalciuria, childhood, self-limiting Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Childhood hypophosphatasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alternating hemiplegia of childhood 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophies of Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset. |
Mental Disorders Diagnosed in Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset. |
Alternating hemiplegia of childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset. |
Arthropathy, progressive pseudorheumatoid, of childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset. |
Hypophosphatasia, Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Childhood from the curated CTD Gene-Disease Associations dataset. |
alternating hemiplegia of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
childhood medulloblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood oligodendroglioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood electroclinical syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood type dermatomyositis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood kidney neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood disintegrative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood kidney cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood absence epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alternating hemiplegia of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood pilocytic astrocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe childhood thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood b-cell non-hodgkin's lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute lymphoblastic leukemia (childhood) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute lymphoblastic leukemia (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood asthma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial asthma (childhood only) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temperament in early childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temperament in early childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood absence epilepsy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood b-cell precursor acute lymphoblastic leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood b-cell precursor acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophies of childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumors ; residential insecticide exposure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial asthma (childhood & adult) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood atopic asthma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, childhood acute lymphoblastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute lymphoblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood acute lymphoblastic leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood-onset mood disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood-onset mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood maltreatment Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood maltreatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood asthma. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma (childhood) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, childhood acute; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood idiopathic thrombocytopenic purpura. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma and ige in childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma and ige in childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma (childhood onset) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term childhood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Fractional exhaled nitric oxide (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma (childhood onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Acute lymphoblastic leukemia (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Intelligence (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Intelligence (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma (childhood, severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
childhood-onset short-trunk short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections in infancy and early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood-onset truncal obesity Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood-onset truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset short-limb short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset sensorineural hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inability to walk by childhood/adolescence Gene SetFrom HPO Gene-Disease Associations genes associated with the inability to walk by childhood/adolescence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
platyspondyly (childhood) Gene SetFrom HPO Gene-Disease Associations genes associated with the platyspondyly (childhood) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Spinal Muscular Atrophies of Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lead Poisoning, Nervous System, Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lead Poisoning, Nervous System, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Schizophrenia, Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Schizophrenia, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
hypophosphatasia, childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypophosphatasia, childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatocellular carcinoma, childhood type Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatocellular carcinoma, childhood type phenotype from the curated OMIM Gene-Disease Associations dataset. |
alternating hemiplegia of childhood 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, childhood absence, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
transient erythroblastopenia of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the transient erythroblastopenia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, reducing body, x-linked, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis, north american indian childhood type Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset. |
alternating hemiplegia of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthropathy, progressive pseudorheumatoid, of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyarteritis nodosa, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyarteritis nodosa, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neurodegeneration with optic atrophy, childhood onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epileptic encephalopathy, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Liposarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Neuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Kidney Wilms Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Cytopenia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Absence Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Megakaryoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Megakaryoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Soft Part Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diffuse Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nephrotic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pilocytic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Synovial Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Synovial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood T Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Newly Diagnosed Childhood Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Newly Diagnosed Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Metastatic Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Steroid Resistant Nephrotic Syndrome Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Steroid Resistant Nephrotic Syndrome Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Undifferentiated Pleomorphic Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Undifferentiated Pleomorphic Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Asthma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Supratentorial Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Monocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myelomonocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myelomonocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Burkitt Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hematopoietic Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hematopoietic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pre-B Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pre-B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Oligodendroglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ataxia With Central Nervous System Hypomyelinization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Craniopharyngioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Eosinophilic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Eosinophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Embryonal Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ganglioneuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioneuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Leiomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leiomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyarteritis Nodosa, Childhood-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyarteritis Nodosa, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Stem Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Cerebral Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gliosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Angiosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Testicular Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ganglioglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Teratoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Childhood Caries Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Promyelocytic Leukemia With Pml-Rara Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Promyelocytic Leukemia With Pml-Rara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pleomorphic Xanthoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood T Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Onset Dystonias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Onset Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hypophosphatasia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hypophosphatasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Subependymal Giant Cell Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Subependymal Giant Cell Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Oligoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Oligodendroglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade I Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade I Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Langerhans Cell Histiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Atopic Dermatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pineoblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pineoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Monoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Clear Cell Sarcoma Of Soft Parts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Clear Cell Sarcoma Of Soft Parts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Immunoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diffuse Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Oligoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pilomyxoid Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilomyxoid Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Giant Cell Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Giant Cell Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Fibrillary Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Fibrillary Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Desmoplastic Small Round Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Kidney Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Atypical Teratoid/Rhabdoid Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Stem Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gliomatosis Cerebri Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliomatosis Cerebri in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Thyroid Gland Papillary Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Papillary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ovarian Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ovarian Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Epithelioid Hemangioendothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Hemangioendothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Hemangiopericytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Hemangiopericytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pleomorphic Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood L2 Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood L2 Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Mesenchymal Chondrosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mesenchymal Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Erythroid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Erythroid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Liver Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontal Epilepsy, Benign, Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease North American Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercalciuria, Childhood, Self-Limiting Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercalciuria, Childhood, Self-Limiting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Transient Erythroblastopenia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Transient Erythroblastopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Necrotizing Encephalopathy Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Basophilic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Basophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia In Remission Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Sclerosis Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Sclerosis Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Botryoid-Type Embryonal Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Botryoid-Type Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Tic Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Psychosis, Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Psychosis, Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinal Muscular Atrophies Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophies Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Bronchiectasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Onset Of Psoriasis In Childhood (1-10 Years) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Onset Of Psoriasis In Childhood (1-10 Years) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Conduct Disorder, Childhood-Onset Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Conduct Disorder, Childhood-Onset Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gemistocytic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gemistocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood-Onset Spasticity With Hyperglycinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Spasticity With Hyperglycinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorea, Childhood-Onset, With Psychomotor Retardation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Childhood-Onset, With Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Celiac Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diabetes Mellitus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade Ii Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Ii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Focal Epilepsy, Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Benign Occipital Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gastrointestinal Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progeria Syndrome, Childhood-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progeria Syndrome, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Fibrous Histiocytoma Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Fibrous Histiocytoma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Small Intestinal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Small Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Colorectal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Thyroid Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade Iii Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Iii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Mixed Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Childhood Epilepsy, Myoclonic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Supratentorial Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Early Childhood Onset Retinal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Leukemia In Remission Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Infratentorial Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Infratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Disintegrative Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Disintegrative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Progressive Bulbar Palsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pneumonia Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pneumonia Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Choroid Plexus Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Choroid Plexus Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood-Onset Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Cerebellar Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Onset Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Solid Neoplasm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood-Onset Truncal Obesity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood-Onset Truncal Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Overweight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Overweight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Aggression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Aggression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Selective Mutism Specific To Childhood And Adolescence Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Selective Mutism Specific To Childhood And Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections In Infancy And Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk In Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Onset Short-Limb Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Convulsion In Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Convulsion In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inability To Walk By Childhood/Adolescence Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inability To Walk By Childhood/Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Onset Sensorineural Hearing Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood electroclinical syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Childhood absence epilepsy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Progressive pseudorheumatoid arthropathy of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Childhood type dermatomyositis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Childhood type dermatomyositis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute lymphocytic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood electroclinical syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood B-cell acute lymphoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood B-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood fibrosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood low-grade glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood low-grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood absence epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood disintegrative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood medulloblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute myeloid leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood type dermatomyositis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Systemic Epstein-Barr virus positive T-cell lymphoma of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Systemic Epstein-Barr virus positive T-cell lymphoma of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood T-cell acute lymphoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood T-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood brain stem neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood brain stem glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood germ cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood astrocytic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood astrocytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood infratentorial ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood leptomeningeal melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leptomeningeal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood angiosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood pilocytic astrocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dystonia 28, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood hypophosphatasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset neurodegeneration with brain atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood hepatocellular carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hepatocellular carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood oligodendroglioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute megakaryoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute megakaryoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dystonia 35, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Progressive pseudorheumatoid arthropathy of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood liposarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood supratentorial ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood supratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood testicular germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant childhood germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant childhood germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood infratentorial neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood optic nerve glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney angiomyolipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ovarian dysgerminoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian dysgerminoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ovarian germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood onset hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood apraxia of speech Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood apraxia of speech phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-childhood-onset retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glaucoma of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glaucoma of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood hypophosphatasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset GLUT1 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood neoplasm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood neoplasm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe underweight in infancy childhood and adolescence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe underweight in infancy childhood and adolescence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood ganglioglioma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood ganglioglioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood myocerebrohepatopathy spectrum Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood myocerebrohepatopathy spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive bulbar palsy of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood Onset Dystonias Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset Dystonias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood kidney cell carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood kidney cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive childhood encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood-onset motor and cognitive regression syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile or childhood onset neurodegenerative disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood absence epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary North American Indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary North American Indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood-onset autosomal recessive myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
B-cell childhood acute lymphoblastic leukemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the B-cell childhood acute lymphoblastic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset sensorineural hearing impairment Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood Onset VCP-related Neurodevelopmental Disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset VCP-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Disabling pansclerotic morphea of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Disabling pansclerotic morphea of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Benign childhood epilepsy with centro-temporal spikes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cutaneous mastocytosis (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous mastocytosis (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
First fracture in long-term childhood cancer survivors (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First fracture in long-term childhood cancer survivors (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anthracycline-induced cardiotoxicity in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anthracycline-induced cardiotoxicity in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Obesity in adult survivors of childhood cancer exposed to cranial radiation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Obesity in adult survivors of childhood cancer not exposed to cranial radiation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer not exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Early childhood aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early childhood aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Middle childhood and early adolescence aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood and early adolescence aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood ear infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ear infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood maltreatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood maltreatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Meningococcal C functional antibody titers post childhood immunization Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (childhood onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma onset (childhood vs adult) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma onset (childhood vs adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood onset ulcerative colitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset ulcerative colitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fractional exhaled nitric oxide (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fasting plasma glucose (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting plasma glucose (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (time to childhood onset) x early life tobacco smoke interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) x early life tobacco smoke interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood onset type 2 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood asthma with severe exacerbations Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia in childhood (B cell precursor) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia in childhood (B cell precursor) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Premature menopause in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Premature menopause in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood steroid-sensitive nephrotic syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood steroid-sensitive nephrotic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to placebo treatment in childhood asthma (FVC change) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to placebo treatment in childhood asthma (FVC change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Self-reported childhood asthma in adult smokers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported childhood asthma in adult smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia (adult vs childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (adult vs childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe exacerbations in childhood asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood dental caries in primary teeth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in primary teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood dental caries in permanent teeth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in permanent teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood absence epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cisplatin-induced hearing loss in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |