Name

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.

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.

imbalanced hemoglobin synthesis Gene Set

From HPO Gene-Disease Associations

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

increased expression of the g gamma and a gamma globin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased expression of the g gamma and a gamma globin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombocytopenia due to platelet alloimmunization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

imbalanced Gene Set

From GeneRIF Biological Term Annotations

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

globin Gene Set

From GeneRIF Biological Term Annotations

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

Globin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Globin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Globin Gene Set

From InterPro Predicted Protein Domain Annotations

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

Globin, lamprey/hagfish type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Globin, lamprey/hagfish type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Globin, structural domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Globin, structural domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

Hemolysis Gene Set

From CTD Gene-Disease Associations

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

alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fever; hemolysis; inflammation Gene Set

From GAD Gene-Disease Associations

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

glycogen storage disease type i; hemolysis; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glycogen storage disease type i; hemolysis; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bilirubin; hemolysis Gene Set

From GAD Gene-Disease Associations

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

favism; glucosephosphate dehydrogenase deficiency; hemolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease favism; glucosephosphate dehydrogenase deficiency; hemolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemolysis Gene Set

From GeneRIF Biological Term Annotations

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

hemolysis in other organism Gene Set

From GO Biological Process Annotations

genes participating in the hemolysis in other organism biological process from the curated GO Biological Process Annotations dataset.

hemolysis by symbiont of host erythrocytes Gene Set

From GO Biological Process Annotations

genes participating in the hemolysis by symbiont of host erythrocytes biological process from the curated GO Biological Process Annotations dataset.

hemolysis in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the hemolysis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

exercise-induced hemolysis Gene Set

From HPO Gene-Disease Associations

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

increased red cell hemolysis by shear stress Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red cell hemolysis by shear stress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hemolysis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hemolysis Gene Set

From MPO Gene-Phenotype Associations

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

Absent radii and thrombocytopenia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Absent radii and thrombocytopenia from the curated CTD Gene-Disease Associations 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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

?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.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

congenital goiter and defective tg synthesis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital goiter and defective tg synthesis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

synthesis and degradation of ketone bodies Gene Set

From KEGG Pathways

proteins participating in the synthesis and degradation of ketone bodies pathway from the KEGG Pathways dataset.

Synthesis of IP3 and IP4 in the cytosol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of IP3 and IP4 in the cytosol pathway from the Reactome Pathways dataset.

Gap-filling DNA repair synthesis and ligation in GG-NER Gene Set

From Reactome Pathways

proteins participating in the Gap-filling DNA repair synthesis and ligation in GG-NER pathway from the Reactome Pathways dataset.

Amino acid synthesis and interconversion (transamination) Gene Set

From Reactome Pathways

proteins participating in the Amino acid synthesis and interconversion (transamination) pathway from the Reactome Pathways dataset.

Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) pathway from the Reactome Pathways dataset.

Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.

Synthesis of Leukotrienes (LT) and Eoxins (EX) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Leukotrienes (LT) and Eoxins (EX) pathway from the Reactome Pathways dataset.

Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation Gene Set

From Reactome Pathways

proteins participating in the Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation pathway from the Reactome Pathways dataset.

Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol pathway from the Reactome Pathways dataset.

Synthesis And Processing Of GAG, GAGPOL Polyproteins Gene Set

From Reactome Pathways

proteins participating in the Synthesis And Processing Of GAG, GAGPOL Polyproteins pathway from the Reactome Pathways dataset.

Incretin synthesis, secretion, and inactivation Gene Set

From Reactome Pathways

proteins participating in the Incretin synthesis, secretion, and inactivation pathway from the Reactome Pathways dataset.

Synthesis of IP2, IP, and Ins in the cytosol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of IP2, IP, and Ins in the cytosol pathway from the Reactome Pathways dataset.

Transport and synthesis of PAPS Gene Set

From Reactome Pathways

proteins participating in the Transport and synthesis of PAPS pathway from the Reactome Pathways dataset.

Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) Gene Set

From Reactome Pathways

proteins participating in the Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) pathway from the Reactome Pathways dataset.

Synthesis of bile acids and bile salts Gene Set

From Reactome Pathways

proteins participating in the Synthesis of bile acids and bile salts pathway from the Reactome Pathways dataset.

GABA synthesis, release, reuptake and degradation Gene Set

From Reactome Pathways

proteins participating in the GABA synthesis, release, reuptake and degradation pathway from the Reactome Pathways dataset.

Synthesis of Hepoxilins (HX) and Trioxilins (TrX) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Hepoxilins (HX) and Trioxilins (TrX) pathway from the Reactome Pathways dataset.

Synthesis of bile acids and bile salts via 24-hydroxycholesterol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of bile acids and bile salts via 24-hydroxycholesterol pathway from the Reactome Pathways dataset.

Glutathione synthesis and recycling Gene Set

From Reactome Pathways

proteins participating in the Glutathione synthesis and recycling pathway from the Reactome Pathways dataset.

Synthesis of Prostaglandins (PG) and Thromboxanes (TX) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Prostaglandins (PG) and Thromboxanes (TX) pathway from the Reactome Pathways dataset.

Synthesis, secretion, and deacylation of Ghrelin Gene Set

From Reactome Pathways

proteins participating in the Synthesis, secretion, and deacylation of Ghrelin pathway from the Reactome Pathways dataset.

Gap-filling DNA repair synthesis and ligation in TC-NER Gene Set

From Reactome Pathways

proteins participating in the Gap-filling DNA repair synthesis and ligation in TC-NER pathway from the Reactome Pathways dataset.

Synthesis of bile acids and bile salts via 27-hydroxycholesterol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of bile acids and bile salts via 27-hydroxycholesterol pathway from the Reactome Pathways dataset.

Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. Gene Set

From Reactome Pathways

proteins participating in the Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. pathway from the Reactome Pathways dataset.

Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) Gene Set

From Reactome Pathways

proteins participating in the Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) pathway from the Reactome Pathways dataset.

Prostaglandin Synthesis and Regulation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Prostaglandin Synthesis and Regulation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Synthesis and Degradation of Ketone Bodies(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Synthesis and Degradation of Ketone Bodies(Mus musculus) pathway from the Wikipathways Pathways dataset.

Prostaglandin Synthesis and Regulation(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Prostaglandin Synthesis and Regulation(Mus musculus) pathway from the Wikipathways Pathways dataset.

Synthesis and Degradation of Ketone Bodies(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Synthesis and Degradation of Ketone Bodies(Homo sapiens) pathway from the Wikipathways Pathways dataset.

platelet reactivity and clopidogrel resistance Gene Set

From GAD Gene-Disease Associations

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

double homozygosity for receptor polymorphisms of platelet gpia and gpiiia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double homozygosity for receptor polymorphisms of platelet gpia and gpiiia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet receptor density and the response to sfllrn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet receptor density and the response to sfllrn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

Factors involved in megakaryocyte development and platelet production Gene Set

From Reactome Pathways

proteins participating in the Factors involved in megakaryocyte development and platelet production pathway from the Reactome Pathways dataset.

Platelet activation, signaling and aggregation Gene Set

From Reactome Pathways

proteins participating in the Platelet activation, signaling and aggregation pathway from the Reactome Pathways dataset.

Thrombocytopenia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Radial aplasia-thrombocytopenia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GATA-1-related thrombocytopenia with dyserythropoiesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GATA-1-related thrombocytopenia with dyserythropoiesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, X-linked, intermittent Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, X-linked, intermittent phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THROMBOCYTOPENIA 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA 2 from the curated CTD Gene-Disease Associations dataset.

Thrombocytopenia Gene Set

From CTD Gene-Disease Associations

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

Thrombocytopenia 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombocytopenia 1 from the curated CTD Gene-Disease Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From CTD Gene-Disease Associations

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

Thrombocytopenia 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombocytopenia 4 from the curated CTD Gene-Disease Associations dataset.

Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

Thrombocytopenia, Neonatal Alloimmune Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombocytopenia, Neonatal Alloimmune from the curated CTD Gene-Disease Associations dataset.

Thrombocytopenia Paris-Trousseau type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombocytopenia Paris-Trousseau type from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia-absent radius syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease thrombocytopenia-absent radius syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

acquired thrombocytopenia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thrombocytopenia-absent radius syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

primary thrombocytopenia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thrombocytopenia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

transient neonatal thrombocytopenia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mucositis; neoplasm, residual; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mucositis; neoplasm, residual; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; neutropenia; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

dengue; dengue hemorrhagic fever; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; proteinuria; rheumatoid arthritis; rheumatoid nodule; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; proteinuria; rheumatoid arthritis; rheumatoid nodule; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neonatal thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

heparin-induced thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

x-linked thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

thrombocytopenia; thrombosis Gene Set

From GAD Gene-Disease Associations

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

neutropenia; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neutropenia; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

hematologic diseases; neutropenia; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

kidney diseases; lupus erythematosus, systemic; systemic lupus erythematosus; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

thrombocytopenia Gene Set

From GeneRIF Biological Term Annotations

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

thrombocytopenia Gene Set

From GWASdb SNP-Disease Associations

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

intermittent thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

neonatal alloimmune thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

autoimmune thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

amegakaryocytic thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

congenital thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

post-transfusion thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

thrombocytopenia Gene Set

From HPO Gene-Disease Associations

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

Thrombocytopenia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Thrombocytopenia, Neonatal Alloimmune Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Thrombocytopenia, Neonatal Alloimmune phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

thrombocytopenia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked Gene Set

From OMIM Gene-Disease Associations

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

thrombocytopenia, x-linked, intermittent Gene Set

From OMIM Gene-Disease Associations

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

radioulnar synostosis with amegakaryocytic thrombocytopenia Gene Set

From OMIM Gene-Disease Associations

genes associated with the radioulnar synostosis with amegakaryocytic thrombocytopenia phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, neonatal alloimmune Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia with beta-thalassemia, x-linked Gene Set

From OMIM Gene-Disease Associations

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

thrombocytopenia-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, neonatal alloimmune, bak antigen related Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, neonatal alloimmune, bak antigen related phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia-absent radius syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia-absent radius syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

?thrombocytopenia, paris-trousseau type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?thrombocytopenia, paris-trousseau type phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, congenital amegakaryocytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, congenital amegakaryocytic phenotype from the curated OMIM Gene-Disease Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 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.

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.

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.

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.

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.

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.

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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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.

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.

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.

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.

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.

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.

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.

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.

srebp control of lipid synthesis Gene Set

From Biocarta Pathways

proteins participating in the srebp control of lipid synthesis pathway from the Biocarta Pathways dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cholesterol synthesis rate Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; bile acid synthesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; bile acid synthesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

interleukin-1 beta (il-1 beta) synthesis capacity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease interleukin-1 beta (il-1 beta) synthesis capacity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytokine synthesis Gene Set

From GAD Gene-Disease Associations

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

synthesisof Gene Set

From GeneRIF Biological Term Annotations

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

synthesised Gene Set

From GeneRIF Biological Term Annotations

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

synthesisdependent Gene Set

From GeneRIF Biological Term Annotations

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

synthesisdegradation Gene Set

From GeneRIF Biological Term Annotations

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

synthesis Gene Set

From GeneRIF Biological Term Annotations

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

synthesisindependent Gene Set

From GeneRIF Biological Term Annotations

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

synthesissecretion Gene Set

From GeneRIF Biological Term Annotations

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

synthesiscell Gene Set

From GeneRIF Biological Term Annotations

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

dna synthesis involved in dna repair Gene Set

From GO Biological Process Annotations

genes participating in the dna synthesis involved in dna repair biological process from the curated GO Biological Process Annotations dataset.

trna dihydrouridine synthesis Gene Set

From GO Biological Process Annotations

genes participating in the trna dihydrouridine synthesis biological process from the curated GO Biological Process Annotations dataset.

atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

rrna pseudouridine synthesis Gene Set

From GO Biological Process Annotations

genes participating in the rrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations dataset.

error-prone translesion synthesis Gene Set

From GO Biological Process Annotations

genes participating in the error-prone translesion synthesis biological process from the curated GO Biological Process Annotations dataset.

snrna pseudouridine synthesis Gene Set

From GO Biological Process Annotations

genes participating in the snrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations dataset.

mrna pseudouridine synthesis Gene Set

From GO Biological Process Annotations

genes participating in the mrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations dataset.

dna replication, synthesis of rna primer Gene Set

From GO Biological Process Annotations

genes participating in the dna replication, synthesis of rna primer biological process from the curated GO Biological Process Annotations dataset.

pseudouridine synthesis Gene Set

From GO Biological Process Annotations

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

translesion synthesis Gene Set

From GO Biological Process Annotations

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

meiotic dna repair synthesis Gene Set

From GO Biological Process Annotations

genes participating in the meiotic dna repair synthesis biological process from the curated GO Biological Process Annotations dataset.

trna pseudouridine synthesis Gene Set

From GO Biological Process Annotations

genes participating in the trna pseudouridine synthesis biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

reduced beta/alpha synthesis ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced beta/alpha synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced alpha/beta synthesis ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced alpha/beta synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fructose 2,6-bisphosphate synthesis/dephosphorylation Gene Set

From HumanCyc Pathways

proteins participating in the fructose 2,6-bisphosphate synthesis/dephosphorylation pathway from the HumanCyc Pathways dataset.

Diphthamide synthesis DHP2, eukaryotic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Diphthamide synthesis DHP2, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor synthesis C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor synthesis C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

tRNA wybutosine-synthesis Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the tRNA wybutosine-synthesis protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Synthesis of cytochrome c oxidase, Sco1/Sco2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Synthesis of cytochrome c oxidase, Sco1/Sco2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Diphthamide synthesis DPH1/DPH2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Diphthamide synthesis DPH1/DPH2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal mitochondrial atp synthesis coupled electron transport Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial atp synthesis coupled electron transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bile acid synthesis defect, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

Vasopressin synthesis Gene Set

From PANTHER Pathways

proteins participating in the Vasopressin synthesis pathway from the PANTHER Pathways dataset.

Gamma-aminobutyric acid synthesis Gene Set

From PANTHER Pathways

proteins participating in the Gamma-aminobutyric acid synthesis pathway from the PANTHER Pathways dataset.

ATP synthesis Gene Set

From PANTHER Pathways

proteins participating in the ATP synthesis pathway from the PANTHER Pathways dataset.

Histamine synthesis Gene Set

From PANTHER Pathways

proteins participating in the Histamine synthesis pathway from the PANTHER Pathways dataset.

Telomere C-strand synthesis initiation Gene Set

From Reactome Pathways

proteins participating in the Telomere C-strand synthesis initiation pathway from the Reactome Pathways dataset.

Synthesis of GDP-mannose Gene Set

From Reactome Pathways

proteins participating in the Synthesis of GDP-mannose pathway from the Reactome Pathways dataset.

Hypusine synthesis from eIF5A-lysine Gene Set

From Reactome Pathways

proteins participating in the Hypusine synthesis from eIF5A-lysine pathway from the Reactome Pathways dataset.

Synthesis of dolichyl-phosphate-glucose Gene Set

From Reactome Pathways

proteins participating in the Synthesis of dolichyl-phosphate-glucose pathway from the Reactome Pathways dataset.

Synthesis of PS Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PS pathway from the Reactome Pathways dataset.

Synthesis of PE Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PE pathway from the Reactome Pathways dataset.

GABA synthesis Gene Set

From Reactome Pathways

proteins participating in the GABA synthesis pathway from the Reactome Pathways dataset.

Translesion synthesis by DNA polymerases bypassing lesion on DNA template Gene Set

From Reactome Pathways

proteins participating in the Translesion synthesis by DNA polymerases bypassing lesion on DNA template pathway from the Reactome Pathways dataset.

Synthesis of IPs in the ER lumen Gene Set

From Reactome Pathways

proteins participating in the Synthesis of IPs in the ER lumen pathway from the Reactome Pathways dataset.

Minus-strand DNA synthesis Gene Set

From Reactome Pathways

proteins participating in the Minus-strand DNA synthesis pathway from the Reactome Pathways dataset.

Post-translational modification: synthesis of GPI-anchored proteins Gene Set

From Reactome Pathways

proteins participating in the Post-translational modification: synthesis of GPI-anchored proteins pathway from the Reactome Pathways dataset.

A tetrasaccharide linker sequence is required for GAG synthesis Gene Set

From Reactome Pathways

proteins participating in the A tetrasaccharide linker sequence is required for GAG synthesis pathway from the Reactome Pathways dataset.

Synthesis of substrates in N-glycan biosythesis Gene Set

From Reactome Pathways

proteins participating in the Synthesis of substrates in N-glycan biosythesis pathway from the Reactome Pathways dataset.

Viral Messenger RNA Synthesis Gene Set

From Reactome Pathways

proteins participating in the Viral Messenger RNA Synthesis pathway from the Reactome Pathways dataset.

Synthesis of DNA Gene Set

From Reactome Pathways

proteins participating in the Synthesis of DNA pathway from the Reactome Pathways dataset.

Carnitine synthesis Gene Set

From Reactome Pathways

proteins participating in the Carnitine synthesis pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the early endosome membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways dataset.

Glycogen synthesis Gene Set

From Reactome Pathways

proteins participating in the Glycogen synthesis pathway from the Reactome Pathways dataset.

Synthesis of Ketone Bodies Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Ketone Bodies pathway from the Reactome Pathways dataset.

Translesion synthesis by Pol eta Gene Set

From Reactome Pathways

proteins participating in the Translesion synthesis by Pol eta pathway from the Reactome Pathways dataset.

Synthesis of IPs in the nucleus Gene Set

From Reactome Pathways

proteins participating in the Synthesis of IPs in the nucleus pathway from the Reactome Pathways dataset.

Processive synthesis on the lagging strand Gene Set

From Reactome Pathways

proteins participating in the Processive synthesis on the lagging strand pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis of glycosylphosphatidylinositol (GPI) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of glycosylphosphatidylinositol (GPI) pathway from the Reactome Pathways dataset.

Synthesis of 5-eicosatetraenoic acids Gene Set

From Reactome Pathways

proteins participating in the Synthesis of 5-eicosatetraenoic acids pathway from the Reactome Pathways dataset.

Translesion synthesis by HREV1 Gene Set

From Reactome Pathways

proteins participating in the Translesion synthesis by HREV1 pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the Golgi membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the Golgi membrane pathway from the Reactome Pathways dataset.

Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) pathway from the Reactome Pathways dataset.

Insulin effects increased synthesis of Xylulose-5-Phosphate Gene Set

From Reactome Pathways

proteins participating in the Insulin effects increased synthesis of Xylulose-5-Phosphate pathway from the Reactome Pathways dataset.

Synthesis of 12-eicosatetraenoic acid derivatives Gene Set

From Reactome Pathways

proteins participating in the Synthesis of 12-eicosatetraenoic acid derivatives pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the late endosome membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the late endosome membrane pathway from the Reactome Pathways dataset.

Repair synthesis for gap-filling by DNA polymerase in TC-NER Gene Set

From Reactome Pathways

proteins participating in the Repair synthesis for gap-filling by DNA polymerase in TC-NER pathway from the Reactome Pathways dataset.

Synthesis of UDP-N-acetyl-glucosamine Gene Set

From Reactome Pathways

proteins participating in the Synthesis of UDP-N-acetyl-glucosamine pathway from the Reactome Pathways dataset.

Synthesis of 15-eicosatetraenoic acid derivatives Gene Set

From Reactome Pathways

proteins participating in the Synthesis of 15-eicosatetraenoic acid derivatives pathway from the Reactome Pathways dataset.

Synthesis of PA Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PA pathway from the Reactome Pathways dataset.

Synthesis of PC Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PC pathway from the Reactome Pathways dataset.

Synthesis of PG Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PG pathway from the Reactome Pathways dataset.

Synthesis of PI Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PI pathway from the Reactome Pathways dataset.

Synthesis of PIPs at the ER membrane Gene Set

From Reactome Pathways

proteins participating in the Synthesis of PIPs at the ER membrane pathway from the Reactome Pathways dataset.

Synthesis of pyrophosphates in the cytosol Gene Set

From Reactome Pathways

proteins participating in the Synthesis of pyrophosphates in the cytosol pathway from the Reactome Pathways dataset.

Reactions specific to the complex N-glycan synthesis pathway Gene Set

From Reactome Pathways

proteins participating in the Reactions specific to the complex N-glycan synthesis pathway pathway from the Reactome Pathways dataset.

Reactions specific to the hybrid N-glycan synthesis pathway Gene Set

From Reactome Pathways

proteins participating in the Reactions specific to the hybrid N-glycan synthesis pathway pathway from the Reactome Pathways dataset.

Synthesis of Dolichyl-phosphate Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Dolichyl-phosphate pathway from the Reactome Pathways dataset.

Processive synthesis on the C-strand of the telomere Gene Set

From Reactome Pathways

proteins participating in the Processive synthesis on the C-strand of the telomere pathway from the Reactome Pathways dataset.

Lagging Strand Synthesis Gene Set

From Reactome Pathways

proteins participating in the Lagging Strand Synthesis pathway from the Reactome Pathways dataset.

Synthesis of diphthamide-EEF2 Gene Set

From Reactome Pathways

proteins participating in the Synthesis of diphthamide-EEF2 pathway from the Reactome Pathways dataset.

Leading Strand Synthesis Gene Set

From Reactome Pathways

proteins participating in the Leading Strand Synthesis pathway from the Reactome Pathways dataset.

Synthesis of Lipoxins (LX) Gene Set

From Reactome Pathways

proteins participating in the Synthesis of Lipoxins (LX) pathway from the Reactome Pathways dataset.

Plus-strand DNA synthesis Gene Set

From Reactome Pathways

proteins participating in the Plus-strand DNA synthesis pathway from the Reactome Pathways dataset.

Synthesis of dolichyl-phosphate mannose Gene Set

From Reactome Pathways

proteins participating in the Synthesis of dolichyl-phosphate mannose pathway from the Reactome Pathways dataset.

Translesion synthesis by Pol zeta Gene Set

From Reactome Pathways

proteins participating in the Translesion synthesis by Pol zeta pathway from the Reactome Pathways dataset.

Synthesis of CL Gene Set

From Reactome Pathways

proteins participating in the Synthesis of CL pathway from the Reactome Pathways dataset.

Repair synthesis of patch ~27-30 bases long by DNA polymerase Gene Set

From Reactome Pathways

proteins participating in the Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway from the Reactome Pathways dataset.

Telomere C-strand (Lagging Strand) Synthesis Gene Set

From Reactome Pathways

proteins participating in the Telomere C-strand (Lagging Strand) Synthesis pathway from the Reactome Pathways dataset.

Synthesis of very long-chain fatty acyl-CoAs Gene Set

From Reactome Pathways

proteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset.

Biogenic Amine Synthesis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Biogenic Amine Synthesis(Mus musculus) pathway from the Wikipathways Pathways dataset.

Triacylglyceride Synthesis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Triacylglyceride Synthesis(Mus musculus) pathway from the Wikipathways Pathways dataset.

Biogenic Amine Synthesis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Biogenic Amine Synthesis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Acetylcholine Synthesis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Acetylcholine Synthesis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Acetylcholine Synthesis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Acetylcholine Synthesis(Mus musculus) pathway from the Wikipathways Pathways dataset.

Eicosanoid Synthesis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Eicosanoid Synthesis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Triacylglyceride Synthesis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Triacylglyceride Synthesis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Eicosanoid Synthesis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Eicosanoid Synthesis(Mus musculus) pathway from the Wikipathways Pathways dataset.

platelet amyloid precursor protein pathway Gene Set

From Biocarta Pathways

proteins participating in the platelet amyloid precursor protein pathway pathway from the Biocarta Pathways dataset.

aspirin blocks signaling pathway involved in platelet activation Gene Set

From Biocarta Pathways

proteins participating in the aspirin blocks signaling pathway involved in platelet activation pathway from the Biocarta Pathways dataset.

Platelet-activating factor acetylhydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-activating factor acetylhydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet glycoprotein IV deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet glycoprotein IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gray platelet syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gray platelet syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial platelet disorder with associated myeloid malignancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bleeding disorder, platelet-type, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bleeding disorder, platelet-type, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bleeding disorder, platelet-type, 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bleeding disorder, platelet-type, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

platelet alpha granule membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet alpha granule membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense granule membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense granule membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet alpha granule lumen Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet alpha granule lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense tubular network membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense tubular network membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet alpha granule Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet alpha granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense tubular network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense tubular network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense granule Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet alpha granule membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the platelet alpha granule membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

platelet dense granule membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the platelet dense granule membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

platelet alpha granule Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the platelet alpha granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

platelet dense granule Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the platelet dense granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Platelet Activating Factor Gene Set

From CTD Gene-Chemical Interactions

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

Platelet Glycoprotein IV Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platelet Glycoprotein IV Deficiency from the curated CTD Gene-Disease Associations dataset.

Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.

Von Willebrand disease, platelet type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset.

Gray Platelet Syndrome Gene Set

From CTD Gene-Disease Associations

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

BLEEDING DISORDER, PLATELET-TYPE, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BLEEDING DISORDER, PLATELET-TYPE, 8 from the curated CTD Gene-Disease Associations dataset.

Blood Platelet Disorders Gene Set

From CTD Gene-Disease Associations

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

Platelet Aggregation Gene Set

From dbGAP Gene-Trait Associations

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

Platelet Count Gene Set

From dbGAP Gene-Trait Associations

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

blood platelet disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

blood platelet disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

platelet storage pool deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease platelet storage pool deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Platelet Activating Factor Gene Set

From DrugBank Drug Targets

interacting proteins for the Platelet Activating Factor drug from the curated DrugBank Drug Targets dataset.

blood platelet disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

adenosine diphosphate-induced platelet aggregation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenosine diphosphate-induced platelet aggregation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet alpha(2)beta(1), densities of Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet alpha(2)beta(1), densities of in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet phamacodynamics Gene Set

From GAD Gene-Disease Associations

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

platelet monoamine oxidase b activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet monoamine oxidase b activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet signaling Gene Set

From GAD Gene-Disease Associations

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

platelet thrombogenicity Gene Set

From GAD Gene-Disease Associations

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

sticky platelet syndrome Gene Set

From GAD Gene-Disease Associations

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

platelet aggregation Gene Set

From GAD Gene-Disease Associations

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

blood platelet disorders; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

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

coronary artery bypass grafting; platelet hyperreactivity Gene Set

From GAD Gene-Disease Associations

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

quebec platelet disorder Gene Set

From GAD Gene-Disease Associations

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

mean platelet volume Gene Set

From GAD Gene-Disease Associations

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

platelet alpha2 beta1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet alpha2 beta1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet aggregation; thromboxate Gene Set

From GAD Gene-Disease Associations

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

increased platelet aggregability Gene Set

From GAD Gene-Disease Associations

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

variation in platelet integrin alpha 2 beta 1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variation in platelet integrin alpha 2 beta 1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet aggregation; nitric oxide activity Gene Set

From GAD Gene-Disease Associations

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

platelet count Gene Set

From GAD Gene-Disease Associations

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

fibrinogen; platelet aggregability Gene Set

From GAD Gene-Disease Associations

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

platelet Gene Set

From GeneRIF Biological Term Annotations

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

regulation of platelet-derived growth factor production Gene Set

From GO Biological Process Annotations

genes participating in the regulation of platelet-derived growth factor production biological process from the curated GO Biological Process Annotations dataset.

vegf-activated platelet-derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the vegf-activated platelet-derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

platelet-derived growth factor receptor-alpha signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the platelet-derived growth factor receptor-alpha signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of platelet activation Gene Set

From GO Biological Process Annotations

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

platelet degranulation Gene Set

From GO Biological Process Annotations

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

negative regulation of platelet-derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of platelet-derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of platelet-derived growth factor receptor-beta signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations dataset.

platelet activating factor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the platelet activating factor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

platelet morphogenesis Gene Set

From GO Biological Process Annotations

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

negative regulation of platelet aggregation Gene Set

From GO Biological Process Annotations

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

positive regulation of platelet-derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of platelet-derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of platelet-derived growth factor production Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of platelet-derived growth factor production biological process from the curated GO Biological Process Annotations dataset.

platelet-derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the platelet-derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cell proliferation by vegf-activated platelet derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cell proliferation by vegf-activated platelet derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations dataset.

platelet activating factor metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the platelet activating factor metabolic process biological process from the curated GO Biological Process Annotations dataset.

response to platelet-derived growth factor Gene Set

From GO Biological Process Annotations

genes participating in the response to platelet-derived growth factor biological process from the curated GO Biological Process Annotations dataset.

platelet aggregation Gene Set

From GO Biological Process Annotations

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

regulation of platelet-derived growth factor receptor-alpha signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of platelet-derived growth factor receptor-alpha signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of platelet activation Gene Set

From GO Biological Process Annotations

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

negative regulation of platelet-derived growth factor receptor-beta signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of platelet activation Gene Set

From GO Biological Process Annotations

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

platelet dense granule organization Gene Set

From GO Biological Process Annotations

genes participating in the platelet dense granule organization biological process from the curated GO Biological Process Annotations dataset.

cellular response to platelet-derived growth factor stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to platelet-derived growth factor stimulus biological process from the curated GO Biological Process Annotations dataset.

platelet activation Gene Set

From GO Biological Process Annotations

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

positive regulation of platelet aggregation Gene Set

From GO Biological Process Annotations

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

regulation of platelet aggregation Gene Set

From GO Biological Process Annotations

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

negative regulation of platelet-derived growth factor receptor-alpha signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of platelet-derived growth factor receptor-alpha signaling pathway biological process from the curated GO Biological Process Annotations dataset.

platelet alpha granule organization Gene Set

From GO Biological Process Annotations

genes participating in the platelet alpha granule organization biological process from the curated GO Biological Process Annotations dataset.

platelet formation Gene Set

From GO Biological Process Annotations

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

serotonin secretion by platelet Gene Set

From GO Biological Process Annotations

genes participating in the serotonin secretion by platelet biological process from the curated GO Biological Process Annotations dataset.

positive regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations dataset.

phosphatidylserine exposure on blood platelet Gene Set

From GO Biological Process Annotations

genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations dataset.

protein secretion by platelet Gene Set

From GO Biological Process Annotations

genes participating in the protein secretion by platelet biological process from the curated GO Biological Process Annotations dataset.

platelet-derived growth factor receptor-beta signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of platelet-derived growth factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of platelet-derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

platelet alpha granule lumen Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet alpha granule lumen cellular component from the curated GO Cellular Component Annotations dataset.

platelet alpha granule membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet alpha granule membrane cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense granule membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense granule membrane cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense tubular network membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense tubular network membrane cellular component from the curated GO Cellular Component Annotations dataset.

platelet alpha granule Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet alpha granule cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense tubular network Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense tubular network cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense granule Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense granule cellular component from the curated GO Cellular Component Annotations dataset.

platelet activating factor receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the platelet activating factor receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

platelet-derived growth factor alpha-receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the platelet-derived growth factor alpha-receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

platelet-activating factor acetyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the platelet-activating factor acetyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

platelet-derived growth factor binding Gene Set

From GO Molecular Function Annotations

genes performing the platelet-derived growth factor binding molecular function from the curated GO Molecular Function Annotations dataset.

platelet-derived growth factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the platelet-derived growth factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

platelet-derived growth factor beta-receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the platelet-derived growth factor beta-receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

platelet-derived growth factor-activated receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the platelet-derived growth factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Platelet counts Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Mean platelet volume Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Mean platelet volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Platelet aggregation Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

blood platelet disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormal platelet count Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired platelet aggregation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the impaired platelet aggregation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal platelet function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired collagen-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired collagen-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

platelet antibody positive Gene Set

From HPO Gene-Disease Associations

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

impaired adp-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired adp-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet membrane protein expression Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet granules Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet volume Gene Set

From HPO Gene-Disease Associations

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

impaired thrombin-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired thrombin-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet function Gene Set

From HPO Gene-Disease Associations

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

increased mean platelet volume Gene Set

From HPO Gene-Disease Associations

genes associated with the increased mean platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased mean platelet volume Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased mean platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired epinephrine-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired epinephrine-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet count Gene Set

From HPO Gene-Disease Associations

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

impaired platelet aggregation Gene Set

From HPO Gene-Disease Associations

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

decreased platelet glycoprotein iib-iiia Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased platelet glycoprotein iib-iiia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Blood Platelet Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Platelet-activating factor acetylhydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-activating factor acetylhydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor receptor beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor receptor beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-activating factor acetylhydrolase, eucaryote Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-activating factor acetylhydrolase, eucaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor receptor alpha Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor receptor alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor C Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor C protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-derived growth factor, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-derived growth factor, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Platelet-activating factor receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Platelet-activating factor receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased platelet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet dense granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet dense granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased platelet calcium level Gene Set

From MPO Gene-Phenotype Associations

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

decreased platelet serotonin level Gene Set

From MPO Gene-Phenotype Associations

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

increased platelet aggregation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased platelet aggregation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased platelet atp level Gene Set

From MPO Gene-Phenotype Associations

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

increased mean platelet volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mean platelet volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet activation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet activation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet serotonin level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal platelet adp level Gene Set

From MPO Gene-Phenotype Associations

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

decreased platelet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet dense granule number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet dense granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased platelet adp level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal platelet aggregation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet aggregation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased platelet aggregation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased platelet aggregation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet calcium level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal platelet dense granule physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet dense granule physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mean platelet volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mean platelet volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet atp level Gene Set

From MPO Gene-Phenotype Associations

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

platelet glycoprotein iv deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet glycoprotein iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{bleeding disorder, platelet-type, 13, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bleeding disorder, platelet-type, 13, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

mean platelet volume qtl6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mean platelet volume qtl6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mean platelet volume qtl4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mean platelet volume qtl4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mean platelet volume qtl5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mean platelet volume qtl5 phenotype from the curated OMIM Gene-Disease Associations dataset.

giant platelet disorder, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the giant platelet disorder, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder, platelet-type, 16, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder, platelet-type, 16, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder, platelet-type, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder, platelet-type, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder, platelet-type, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder, platelet-type, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder, platelet-type, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder, platelet-type, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

[mean platelet volume qtl3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [mean platelet volume qtl3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[mean platelet volume qtl1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [mean platelet volume qtl1] phenotype from the curated OMIM Gene-Disease Associations dataset.

quebec platelet disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the quebec platelet disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder, platelet-type, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder, platelet-type, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet-activating factor acetylhydrolase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet-activating factor acetylhydrolase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet disorder, familial, with associated myeloid malignancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet disorder, familial, with associated myeloid malignancy phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet plc beta-2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet plc beta-2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

gray platelet syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the gray platelet syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

[mean platelet volume qtl2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [mean platelet volume qtl2] phenotype from the curated OMIM Gene-Disease Associations dataset.

?bleeding disorder, platelet-type, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?bleeding disorder, platelet-type, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

?bleeding disorder, platelet-type, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?bleeding disorder, platelet-type, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

von willebrand disease, platelet-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the von willebrand disease, platelet-type phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet-derived Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Platelet Adhesion to exposed collagen Gene Set

From Reactome Pathways

proteins participating in the Platelet Adhesion to exposed collagen pathway from the Reactome Pathways dataset.

Platelet degranulation Gene Set

From Reactome Pathways

proteins participating in the Platelet degranulation pathway from the Reactome Pathways dataset.

Platelet sensitization by LDL Gene Set

From Reactome Pathways

proteins participating in the Platelet sensitization by LDL pathway from the Reactome Pathways dataset.

Platelet homeostasis Gene Set

From Reactome Pathways

proteins participating in the Platelet homeostasis pathway from the Reactome Pathways dataset.

Platelet calcium homeostasis Gene Set

From Reactome Pathways

proteins participating in the Platelet calcium homeostasis pathway from the Reactome Pathways dataset.

Response to elevated platelet cytosolic Ca2+ Gene Set

From Reactome Pathways

proteins participating in the Response to elevated platelet cytosolic Ca2+ pathway from the Reactome Pathways dataset.

Platelet Aggregation (Plug Formation) Gene Set

From Reactome Pathways

proteins participating in the Platelet Aggregation (Plug Formation) pathway from the Reactome Pathways dataset.

blood platelet Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood platelet from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

blood platelet Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue blood platelet in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

blood platelet Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From CTD Gene-Disease Associations

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

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

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

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multicentric osteolysis, nodulosis and arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with broad thumb and toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas and Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, hiatal hernia and nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined malonic and methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of Beare and Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints and arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

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

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set

From CORUM Protein Complexes

proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.

NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set

From CORUM Protein Complexes

proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.

6S methyltransferase and RG-containing Sm proteins complex Gene Set

From CORUM Protein Complexes

proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.

Remodeling and spacing factor (RSF) complex Gene Set

From CORUM Protein Complexes

proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.

PBAF complex (Polybromo- and BAF containing complex) Gene Set

From CORUM Protein Complexes

proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.

Cleavage and polyadenylation factor (CPSF) Gene Set

From CORUM Protein Complexes

proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Nucleic and chromatin Fanconi complex Gene Set

From CORUM Protein Complexes

proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.

ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set

From CORUM Protein Complexes

proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.

20S methylosome and RG-containing Sm protein complex Gene Set

From CORUM Protein Complexes

proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.

Amino Acids, Peptides, and Proteins Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.

Bile Acids and Salts Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.

Prime and Bond NT Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.

drospirenone and ethinyl estradiol combination Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.

Hypophosphatemic Rickets And Hyperparathyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Synovitis granulomatous with uveitis and cranial neuropathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.

Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

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

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.

Microtia, Hearing Impairment, And Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.

Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis, anal anomalies, and porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Classical Lissencephalies and Subcortical Band Heterotopias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Russe type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.

Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis And Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Signs and Symptoms, Digestive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria and Homocystinuria, CblD Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset.

Head and Neck Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

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

Cataract, Juvenile, With Microcornea And Glucosuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.

HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.

Venous Malformations, Multiple Cutaneous and Mucosal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.

BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.

Postoperative Nausea and Vomiting Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset.

Myopathy with lactic acidosis and sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.

Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ce