Peroxisomal Dysfunction

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Results for "Peroxisomal Dysfunction": 28 genes, 314 gene sets

Name
PECR Gene peroxisomal trans-2-enoyl-CoA reductase Enables signaling receptor binding activity and trans-2-enoyl-CoA reductase (NADPH) activity. Involved in phytol metabolic process. Located in peroxisome. [provided by Alliance of Genome Resources, Mar 2025]
PEX11G Gene peroxisomal biogenesis factor 11 gamma The protein encoded by this gene is a member of the PEX11 family. This family is reported to regulate the number and size of peroxisomes in evolutionarily distant organisms. The protein encoded by this gene may induce clustering of peroxisomes. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]
PEX5L Gene peroxisomal biogenesis factor 5-like Enables peroxisome matrix targeting signal-1 binding activity and small GTPase binding activity. Predicted to be involved in protein import into peroxisome matrix, docking. Predicted to act upstream of or within maintenance of protein location and regulation of membrane potential. Located in cytosol. Part of receptor complex. [provided by Alliance of Genome Resources, Mar 2025]
ECH1 Gene enoyl CoA hydratase 1, peroxisomal This gene encodes a member of the hydratase/isomerase superfamily. The gene product shows high sequence similarity to enoyl-coenzyme A (CoA) hydratases of several species, particularly within a conserved domain characteristic of these proteins. The encoded protein, which contains a C-terminal peroxisomal targeting sequence, localizes to the peroxisome. The rat ortholog, which localizes to the matrix of both the peroxisome and mitochondria, can isomerize 3-trans,5-cis-dienoyl-CoA to 2-trans,4-trans-dienoyl-CoA, indicating that it is a delta3,5-delta2,4-dienoyl-CoA isomerase. This enzyme functions in the auxiliary step of the fatty acid beta-oxidation pathway. Expression of the rat gene is induced by peroxisome proliferators. [provided by RefSeq, Jul 2008]
PXMP2 Gene peroxisomal membrane protein 2, 22kDa Located in peroxisomal membrane. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025]
PXMP4 Gene peroxisomal membrane protein 4, 24kDa Predicted to act upstream of or within ether lipid metabolic process. Located in peroxisomal membrane. [provided by Alliance of Genome Resources, Mar 2025]
PXT1 Gene peroxisomal, testis specific 1 Predicted to be involved in positive regulation of apoptotic process and spermatogenesis. Predicted to be active in nucleus and peroxisome. [provided by Alliance of Genome Resources, Mar 2025]
PEX11A Gene peroxisomal biogenesis factor 11 alpha This gene is a member of the PEX11 family, which is composed of membrane elongation factors involved in regulation of peroxisome maintenance and proliferation. This gene product interacts with peroxisomal membrane protein 19 and may respond to outside stimuli to increase peroxisome abundance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]
PEX11B Gene peroxisomal biogenesis factor 11 beta The protein encoded by this gene facilitates peroxisomal proliferation and interacts with PEX19. The encoded protein is found in the peroxisomal membrane. Several transcript variants, some protein-coding and some not protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012]
LONP2 Gene lon peptidase 2, peroxisomal In human, peroxisomes function primarily to catalyze fatty acid beta-oxidation and, as a by-product, produce hydrogen peroxide and superoxide. The protein encoded by this gene is an ATP-dependent protease that likely plays a role in maintaining overall peroxisome homeostasis as well as proteolytically degrading peroxisomal proteins damaged by oxidation. The protein has an N-terminal Lon N substrate recognition domain, an ATPase domain, a proteolytic domain, and, in some isoforms, a C-terminal peroxisome targeting sequence. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2017]
PEX26 Gene peroxisomal biogenesis factor 26 This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]
LOC100131465 Gene peroxisomal biogenesis factor 5 pseudogene
PEX19 Gene peroxisomal biogenesis factor 19 This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
PEX10 Gene peroxisomal biogenesis factor 10 This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
PEX13 Gene peroxisomal biogenesis factor 13 This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]
PEX14 Gene peroxisomal biogenesis factor 14 This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome. [provided by RefSeq, Jul 2008]
PEX16 Gene peroxisomal biogenesis factor 16 The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008]
PEX12P1 Gene peroxisomal biogenesis factor 12 pseudogene 1
PEX1 Gene peroxisomal biogenesis factor 1 This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
PEX3 Gene peroxisomal biogenesis factor 3 The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
PEX2 Gene peroxisomal biogenesis factor 2 This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
PEX5 Gene peroxisomal biogenesis factor 5 The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
PEX7 Gene peroxisomal biogenesis factor 7 This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008]
PEX6 Gene peroxisomal biogenesis factor 6 This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
SLC25A17 Gene solute carrier family 25 (mitochondrial carrier; peroxisomal* membrane protein, 34kDa), member 17* This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
PEX12 Gene peroxisomal biogenesis factor 12 This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
DECR2 Gene 2,4-dienoyl CoA reductase 2, peroxisomal Enables 2,4-dienoyl-CoA reductase (NADPH) activity and trans-2-enoyl-CoA reductase (NADPH) activity. Involved in unsaturated fatty acid biosynthetic process. Predicted to be located in cytosol and peroxisomal membrane. Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Mar 2025]
PEX39 Gene peroxisomal biogenesis factor 39
Peroxisomal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Bifunctional peroxisomal enzyme deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisomal fatty acyl-coa reductase 1 disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisomal fatty acyl-coa reductase 1 disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
integral component of peroxisomal membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the integral component of peroxisomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
intrinsic component of peroxisomal membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the intrinsic component of peroxisomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
peroxisomal matrix Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the peroxisomal matrix cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
peroxisomal part Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the peroxisomal part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
peroxisomal membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the peroxisomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
peroxisomal matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the peroxisomal matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
peroxisomal part Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the peroxisomal part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
peroxisomal membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the peroxisomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Peroxisomal ACYL-COA oxidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peroxisomal ACYL-COA oxidase deficiency from the curated CTD Gene-Disease Associations dataset.
Peroxisomal Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peroxisomal Disorders from the curated CTD Gene-Disease Associations dataset.
peroxisomal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peroxisomal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
peroxisomal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peroxisomal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peroxisomal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term peroxisomal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
peroxisomal transport Gene Set From GO Biological Process Annotations 2015 genes participating in the peroxisomal transport biological process from the curated GO Biological Process Annotations 2015 dataset.
peroxisomal long-chain fatty acid import Gene Set From GO Biological Process Annotations 2015 genes participating in the peroxisomal long-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset.
peroxisomal membrane transport Gene Set From GO Biological Process Annotations 2015 genes participating in the peroxisomal membrane transport biological process from the curated GO Biological Process Annotations 2015 dataset.
integral component of peroxisomal membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the integral component of peroxisomal membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
peroxisomal matrix Gene Set From GO Cellular Component Annotations 2015 proteins localized to the peroxisomal matrix cellular component from the curated GO Cellular Component Annotations 2015 dataset.
peroxisomal part Gene Set From GO Cellular Component Annotations 2015 proteins localized to the peroxisomal part cellular component from the curated GO Cellular Component Annotations 2015 dataset.
peroxisomal membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the peroxisomal membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
intrinsic component of peroxisomal membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the intrinsic component of peroxisomal membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
peroxisomal fatty-acyl-coa transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the peroxisomal fatty-acyl-coa transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Peroxisomal membrane protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal membrane protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peroxisomal biogenesis factor 11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal biogenesis factor 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peroxisomal testis-specific protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal testis-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peroxisomal membrane protein 14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal membrane protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peroxisomal targeting signal 1 receptor family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal targeting signal 1 receptor family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lon protease homologue 2, peroxisomal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lon protease homologue 2, peroxisomal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Peroxisomal membrane protein 11C, metazoa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxisomal membrane protein 11C, metazoa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisomal acyl-coa oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisomal acyl-coa oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisomal fatty acyl-coa reductase 1 disorder Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisomal fatty acyl-coa reductase 1 disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
Peroxisomal lipid metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Peroxisomal lipid metabolism pathway from the Reactome Pathways dataset.
Peroxisomal beta-oxidation of tetracosanoyl-CoA(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Peroxisomal beta-oxidation of tetracosanoyl-CoA(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Peroxisomal Acyl-Coa Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Acyl-Coa Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroxisomal Biogenesis Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Biogenesis Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bifunctional Peroxisomal Enzyme Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifunctional Peroxisomal Enzyme Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
peroxisomal membrane transport Gene Set From GO Biological Process Annotations 2023 genes participating in the peroxisomal membrane transport biological process from the curated GO Biological Process Annotations 2023 dataset.
peroxisomal transport Gene Set From GO Biological Process Annotations 2023 genes participating in the peroxisomal transport biological process from the curated GO Biological Process Annotations 2023 dataset.
peroxisomal matrix Gene Set From GO Cellular Component Annotations 2023 proteins localized to the peroxisomal matrix cellular component from the curated GO Cellular Component Annotations 2023 dataset.
peroxisomal membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the peroxisomal membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
Peroxisomal beta oxidation of tetracosanoyl CoA Gene Set From WikiPathways Pathways 2024 proteins participating in the Peroxisomal beta oxidation of tetracosanoyl CoA pathway from the WikiPathways Pathways 2024 dataset.
Class I peroxisomal membrane protein import Gene Set From Reactome Pathways 2024 proteins participating in the Class I peroxisomal membrane protein import pathway from the Reactome Pathways 2024 dataset.
Peroxisomal lipid metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Peroxisomal lipid metabolism pathway from the Reactome Pathways 2024 dataset.
Peroxisomal protein import Gene Set From Reactome Pathways 2024 proteins participating in the Peroxisomal protein import pathway from the Reactome Pathways 2024 dataset.
TYSND1 cleaves peroxisomal proteins Gene Set From Reactome Pathways 2024 proteins participating in the TYSND1 cleaves peroxisomal proteins pathway from the Reactome Pathways 2024 dataset.
peroxisomal membrane transport Gene Set From GO Biological Process Annotations 2025 genes participating in the peroxisomal membrane transport biological process from the curated GO Biological Process Annotations 2025 dataset.
peroxisomal transport Gene Set From GO Biological Process Annotations 2025 genes participating in the peroxisomal transport biological process from the curated GO Biological Process Annotations 2025 dataset.
peroxisomal membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the peroxisomal membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
peroxisomal matrix Gene Set From GO Cellular Component Annotations 2025 proteins localized to the peroxisomal matrix cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Peroxisomal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peroxisomal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Peroxisomal biogenesis disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peroxisomal biogenesis disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Peroxisomal acyl-CoA oxidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peroxisomal acyl-CoA oxidase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Peroxisomal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroxisomal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroxisomal biogenesis disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroxisomal biogenesis disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Encephalopathy due to defective mitochondrial and peroxisomal fission 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroxisomal acyl-CoA oxidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroxisomal acyl-CoA oxidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroxisomal membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Peroxisomal membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Peroxisomal matrix Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Peroxisomal matrix cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Peroxisomal importomer complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Peroxisomal importomer complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Peroxisomal matrix Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Peroxisomal matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Peroxisomal membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Peroxisomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Peroxisomal importomer complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Peroxisomal importomer complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Intrinsic component of peroxisomal membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of peroxisomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Integral component of peroxisomal membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of peroxisomal membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Peroxisomal disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisomal disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bifunctional peroxisomal enzyme deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peroxisomal biogenesis disorder 3b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisomal biogenesis disorder 3b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to defective mitochondrial and peroxisomal fission phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensorineural deafness with mild renal dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction from the curated CTD Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phagocyte Bactericidal Dysfunction from the curated CTD Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Dysfunction Syndrome from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Left Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset.
Sexual Dysfunction, Physiological Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sexual Dysfunction, Physiological from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erectile Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Right Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis renal dysfunction cholestasis syndrome from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset.
Sphincter of Oddi Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sphincter of Oddi Dysfunction from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Erectile Dysfunction in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ovarian dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ovarian dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
physiological sexual disorders; sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease physiological sexual disorders; sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; inflammation; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; inflammation; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
biliary atresia; liver diseases; primary graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; erectile dysfunction; hypogonadism Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; erectile dysfunction; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endothelial dysfunction in normal humans. Gene Set From GAD Gene-Disease Associations genes associated with the disease endothelial dysfunction in normal humans. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
left ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease left ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; autonomic nervous system dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; autonomic nervous system dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis-related organ dysfunction and shock after burn injury Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis-related organ dysfunction and shock after burn injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary vascular endothelial dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary vascular endothelial dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; coronary endothelial vasomotor dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; coronary endothelial vasomotor dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; renal dysfunction, posttransplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; renal dysfunction, posttransplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; myocardial dysfunction, non-ischaemic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; myocardial dysfunction, non-ischaemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dysfunction Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dysfunction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sexual dysfunction Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sexual dysfunction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
autonomic bladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic bladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
beta-cell dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the beta-cell dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vestibular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the vestibular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gallbladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the gallbladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autonomic erectile dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic erectile dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
urinary bladder sphincter dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the urinary bladder sphincter dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal tubular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the renal tubular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
orthostatic hypotension due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ventricular Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Posterior Tibial Tendon Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Left Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Left phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Graft Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sexual Dysfunction, Physiological Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sexual Dysfunction, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Right Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
multisystemic smooth muscle dysfunction syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the multisystemic smooth muscle dysfunction syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set From OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
autonomic nervous system dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the autonomic nervous system dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
sinoatrial node dysfunction and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the sinoatrial node dysfunction and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.
sensorineural deafness with mild renal dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
Surfactant Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Metabolism Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysfunction Adrenal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysfunction Adrenal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Microvascular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Microvascular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Memory Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Memory Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculogenic Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculogenic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Diastolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Placental Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bowel Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bowel Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minimal Brain Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minimal Brain Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organ Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organ Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Deficiency Or Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Deficiency Or Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinus Node Dysfunction (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinus Node Dysfunction (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Executive Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Executive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic-Pituitary-Adrenal Axis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic-Pituitary-Adrenal Axis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meibomian Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meibomian Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutrophil Actin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutrophil Actin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Dysfunction Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Dysfunction Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symphysis Pubis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symphysis Pubis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autonomic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Female Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorineural Deafness With Mild Renal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pangastrointestinal System Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pangastrointestinal System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinoatrial Node Dysfunction And Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinoatrial Node Dysfunction And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colonic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Colonic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emotional Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emotional Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phagocyte Bactericidal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Male Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Male Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Segmental Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Segmental Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pineal Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pineal Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Tibial Tendon Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyramidal Tract Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Tract Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonneurogenic Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonneurogenic Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Dysfunction With T-Cell Inactivation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Dysfunction With T-Cell Inactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Dysfunction, Postpartum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Dysfunction, Postpartum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Myocardial Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Myocardial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endothelial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endothelial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Liver Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Liver Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Beta-Cell Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beta-Cell Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Urinary Bladder Sphincter Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Urinary Bladder Sphincter Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postoperative Cognitive Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Cognitive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysfunction Of Lateral Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysfunction Of Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurologic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurologic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Orthostatic Hypotension Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vestibular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vestibular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gastrointestinal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Uterine Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uterine Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Erectile Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Right Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Nervous System Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Nervous System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Abnormality Related To Mitochondrial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Abnormality Related To Mitochondrial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Speech Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Speech Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Primary Graft Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Sweating Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diastolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence Gene Set From WikiPathways Pathways 2024 proteins participating in the NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence pathway from the WikiPathways Pathways 2024 dataset.
SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
ROS in COVID 19 endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the ROS in COVID 19 endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Metabolic dysfunction-associated steatotic liver disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ovarian dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Metabolic dysfunction-associated steatotic liver disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovarian dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction and alcohol associated liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatotic liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatohepatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatohepatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thiamine metabolism dysfunction syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine metabolism dysfunction syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Surfactant metabolism dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Surfactant metabolism dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multisystemic smooth muscle dysfunction syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multisystemic smooth muscle dysfunction syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary Surfactant Metabolism Dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary Surfactant Metabolism Dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diastolic dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diastolic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine Metabolism Dysfunction Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine Metabolism Dysfunction Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Memory dysfunction in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Memory dysfunction in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

PECR Gene

PEX11G Gene

PEX5L Gene

ECH1 Gene

PXMP2 Gene

PXMP4 Gene

PXT1 Gene

PEX11A Gene

PEX11B Gene

LONP2 Gene

PEX26 Gene

LOC100131465 Gene

PEX19 Gene

PEX10 Gene

PEX13 Gene

PEX14 Gene

PEX16 Gene

PEX12P1 Gene

PEX1 Gene

PEX3 Gene

PEX2 Gene

PEX5 Gene

PEX7 Gene

PEX6 Gene

SLC25A17 Gene

PEX12 Gene

DECR2 Gene

PEX39 Gene

Peroxisomal Dysfunction Gene Set

myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set

Bifunctional peroxisomal enzyme deficiency Gene Set

Peroxisomal fatty acyl-coa reductase 1 disorder Gene Set

integral component of peroxisomal membrane Gene Set

intrinsic component of peroxisomal membrane Gene Set

peroxisomal matrix Gene Set

peroxisomal part Gene Set

peroxisomal membrane Gene Set

peroxisomal matrix Gene Set

peroxisomal part Gene Set

peroxisomal membrane Gene Set

Peroxisomal ACYL-COA oxidase deficiency Gene Set

Peroxisomal Disorders Gene Set

peroxisomal disease Gene Set

peroxisomal disease Gene Set

peroxisomal Gene Set

peroxisomal transport Gene Set

peroxisomal long-chain fatty acid import Gene Set

peroxisomal membrane transport Gene Set

integral component of peroxisomal membrane Gene Set

peroxisomal matrix Gene Set

peroxisomal part Gene Set

peroxisomal membrane Gene Set

intrinsic component of peroxisomal membrane Gene Set

peroxisomal fatty-acyl-coa transporter activity Gene Set

Peroxisomal membrane protein 4 Gene Set

Peroxisomal biogenesis factor 11 Gene Set

Peroxisomal testis-specific protein 1 Gene Set

Peroxisomal membrane protein 14 Gene Set

Peroxisomal targeting signal 1 receptor family Gene Set

Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene Set

Lon protease homologue 2, peroxisomal Gene Set

Peroxisomal membrane protein 11C, metazoa Gene Set

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

peroxisomal acyl-coa oxidase deficiency Gene Set

peroxisomal fatty acyl-coa reductase 1 disorder Gene Set

Peroxisomal lipid metabolism Gene Set

Peroxisomal beta-oxidation of tetracosanoyl-CoA(Homo sapiens) Gene Set

Peroxisomal Acyl-Coa Oxidase Deficiency Gene Set

Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder Gene Set

Peroxisomal Biogenesis Disorder Gene Set

Bifunctional Peroxisomal Enzyme Deficiency Gene Set

peroxisomal membrane transport Gene Set

peroxisomal transport Gene Set

peroxisomal matrix Gene Set

peroxisomal membrane Gene Set

Peroxisomal beta oxidation of tetracosanoyl CoA Gene Set

Class I peroxisomal membrane protein import Gene Set

Peroxisomal lipid metabolism Gene Set

Peroxisomal protein import Gene Set