| Name |
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oxidized low-density lipoprotein and cardiolipin autoantibodies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oxidized low-density lipoprotein and cardiolipin autoantibodies 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 SetFrom 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. |
increased prevalence and level of insulin autoantibodies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased prevalence and level of insulin autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes-associated autoantibodies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes-associated autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anti-ro 52-kd autoantibodies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anti-ro 52-kd autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoantibodies Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term autoantibodies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Type 1 diabetes autoantibodies Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Type 1 diabetes autoantibodies phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Type 1 diabetes autoantibodies in high risk HLA genotype individuals (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 1 diabetes autoantibodies in high risk HLA genotype individuals (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
oxidized GTP and dGTP detoxification Gene SetFrom HumanCyc Pathways proteins participating in the oxidized GTP and dGTP detoxification pathway from the HumanCyc Pathways dataset. |
ache, low back; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; low back pain; scoliosis; spinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; acute disease; low back pain; pain; sciatica Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; acute disease; low back pain; pain; sciatica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk displacement; low back pain; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; low back pain; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk displacement; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ache, low back; intervertebral disk degeneration; low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk degeneration; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom 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. |
Cardiolipin Gene Setinteracting proteins for the Cardiolipin drug from the curated DrugBank Drug Targets dataset. |
cardiolipin Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term cardiolipin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiolipin acyl-chain remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiolipin acyl-chain remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiolipin biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiolipin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiolipin hydrolase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the cardiolipin hydrolase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
cardiolipin binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the cardiolipin binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
cardiolipin biosynthesis Gene SetFrom HumanCyc Pathways proteins participating in the cardiolipin biosynthesis pathway from the HumanCyc Pathways dataset. |
cardiolipin biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiolipin biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiolipin acyl-chain remodeling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiolipin acyl-chain remodeling biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiolipin binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the cardiolipin binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
cardiolipin hydrolase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the cardiolipin hydrolase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
cardiolipin synthase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the cardiolipin synthase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
cardiolipin synthase (CMP-forming) Gene SetFrom GO Molecular Function Annotations 2023 genes performing the cardiolipin synthase (CMP-forming) molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
cardiolipin acyl-chain remodeling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiolipin acyl-chain remodeling biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiolipin biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiolipin biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiolipin metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiolipin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiolipin binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the cardiolipin binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
cardiolipin hydrolase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the cardiolipin hydrolase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
cardiolipin synthase (CMP-forming) Gene SetFrom GO Molecular Function Annotations 2025 genes performing the cardiolipin synthase (CMP-forming) molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
periodate-oxidized adenosine Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical periodate-oxidized adenosine from the curated CTD Gene-Chemical Interactions dataset. |
periodate-oxidized adenosine 5'-triphosphate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical periodate-oxidized adenosine 5'-triphosphate from the curated CTD Gene-Chemical Interactions dataset. |
oxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical oxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine from the curated CTD Gene-Chemical Interactions dataset. |
Oxidized Glutathione Disulfide Gene Setinteracting proteins for the Oxidized Glutathione Disulfide drug from the curated DrugBank Drug Targets dataset. |
Double Oxidized Cysteine Gene Setinteracting proteins for the Double Oxidized Cysteine drug from the curated DrugBank Drug Targets dataset. |
oxidized phospholipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oxidized phospholipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oxidized Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term oxidized in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
oxidized base lesion dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized base lesion dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidized pyrimidine nucleobase lesion dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized pyrimidine nucleobase lesion dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidized purine nucleobase lesion dna n-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized purine nucleobase lesion dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidized dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidized purine dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidized purine dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
LDL (oxidized) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the LDL (oxidized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Oxidized glutathione Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Oxidized glutathione metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Oxidized dithiothreitol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Oxidized dithiothreitol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
oxidized purine nucleobase lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized purine nucleobase lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized purine DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized purine DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized pyrimidine DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized pyrimidine DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidized base lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Oxidized glutathione Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Oxidized glutathione metabolite from the MW Gene Metabolite Associations dataset. |
oxidized purine nucleobase lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized purine nucleobase lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized purine DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized purine DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized pyrimidine DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized pyrimidine DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidized base lesion DNA N-glycosylase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Oxidized LDL cholesterol levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Oxidized LDL cholesterol levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene SetFrom 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. |
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene SetFrom 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. |
low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low insulin and cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low insulin and cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high neuroticism and low agreeableness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high neuroticism and low agreeableness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high and low levels of cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high and low levels of cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Low Molecular Weight Proteinuria With Hypercalciuria And Nephrocalcinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Molecular Weight Proteinuria With Hypercalciuria And Nephrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low hand grip strength (60 years and older) (EWGSOP) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low hand grip strength (60 years and older) (EWGSOP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low hand grip strength (60 years and older) (FNIH) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low hand grip strength (60 years and older) (FNIH) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
quantitative variation in lipid and lipoprotein traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum lipoprotein lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum lipoprotein lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Plasma lipoprotein assembly, remodeling, and clearance Gene Setproteins participating in the Plasma lipoprotein assembly, remodeling, and clearance pathway from the Reactome Pathways 2024 dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins 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. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Low Back Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Back Pain from the curated CTD Gene-Disease Associations dataset. |
Cardiac Output, Low Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Output, Low from the curated CTD Gene-Disease Associations dataset. |
Vision, Low Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vision, Low from the curated CTD Gene-Disease Associations dataset. |
low tension glaucoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease low tension glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
low compliance bladder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease low compliance bladder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ache, low back; intervertebral disk displacement; spinal osteophytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low plasma levels of factor viic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low plasma levels of factor viic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, open-angle; low tension glaucoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; low tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high triglyceride/ low hdl cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high triglyceride/ low hdl cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiac output, low Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac output, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low tension glaucoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low amplitude p300 waves Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low amplitude p300 waves in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular degeneration; vision, low Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
longer telomeres at low folate nutritional status Gene SetFrom GAD Gene-Disease Associations genes associated with the disease longer telomeres at low folate nutritional status in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low back pain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low hepatic lipase activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low hepatic lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low cetp activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low cetp activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
very low bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease very low bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
high or low factor xiii specific activity. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease high or low factor xiii specific activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low-level lead exposure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low-level lead exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, open-angle; low tension glaucoma; ocular hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; low tension glaucoma; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
resistance in vitro to low-dose aspirin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease resistance in vitro to low-dose aspirin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low birthweight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low birthweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low expression of nb1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low expression of nb1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiac output, low; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac output, low; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term low in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
response to low light intensity stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to low light intensity stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
low-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
low voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
low-affinity phosphate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low-affinity phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
low-affinity l-arginine transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low-affinity l-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
low-affinity glucose:sodium symporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low-affinity glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
low-affinity basic amino acid transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the low-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Blood pressure measurement (low sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
low alkaline phosphatase Gene SetFrom HPO Gene-Disease Associations genes associated with the low alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low gonadotropins (secondary hypogonadism) Gene SetFrom HPO Gene-Disease Associations genes associated with the low gonadotropins (secondary hypogonadism) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low cholesterol esterification rates Gene SetFrom HPO Gene-Disease Associations genes associated with the low cholesterol esterification rates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-to-normal blood pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the low-to-normal blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-frequency hearing loss Gene SetFrom HPO Gene-Disease Associations genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-molecular-weight proteinuria Gene SetFrom HPO Gene-Disease Associations genes associated with the low-molecular-weight proteinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-frequency sensorineural hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the low-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-set, posteriorly rotated ears Gene SetFrom HPO Gene-Disease Associations genes associated with the low-set, posteriorly rotated ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low anterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the low anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low plasma citrulline Gene SetFrom HPO Gene-Disease Associations genes associated with the low plasma citrulline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low posterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the low posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormally low-pitched voice Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormally low-pitched voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low maternal serum estriol Gene SetFrom HPO Gene-Disease Associations genes associated with the low maternal serum estriol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low urinary cyclic amp response to pth administration Gene SetFrom HPO Gene-Disease Associations genes associated with the low urinary cyclic amp response to pth administration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low back pain Gene SetFrom HPO Gene-Disease Associations genes associated with the low back pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-set ears Gene SetFrom HPO Gene-Disease Associations genes associated with the low-set ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low frustration tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the low frustration tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low hanging columella Gene SetFrom HPO Gene-Disease Associations genes associated with the low hanging columella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-set nipples Gene SetFrom HPO Gene-Disease Associations genes associated with the low-set nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Low Back Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Low Back Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cardiac Output, Low Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiac Output, Low phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Low Tension Glaucoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Low Tension Glaucoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Vision, Low Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Vision, Low phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Low temperature viability protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Low temperature viability protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein-tyrosine phosphatase, low molecular weight Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-tyrosine phosphatase, low molecular weight protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein-tyrosine phosphatase, low molecular weight, mammalian Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-tyrosine phosphatase, low molecular weight, mammalian protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased ly6c low monocyte number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ly6c low monocyte number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
low mean erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the low mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
low sweet preference Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the low sweet preference phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
plasma triglyceride level qtl, low Gene SetFrom OMIM Gene-Disease Associations genes associated with the plasma triglyceride level qtl, low phenotype from the curated OMIM Gene-Disease Associations dataset. |
{low renin hypertension, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {low renin hypertension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
Low Vision Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Vision in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Tension Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Tension Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Malignancy, Low-Grade Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Malignancy, Low-Grade in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Phospholipid-Associated Cholelithiasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Phospholipid-Associated Cholelithiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polymorphous Low Grade Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Low Grade Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Back Pain, Mechanical Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Back Pain, Mechanical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infant, Very Low Birth Weight Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infant, Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Squamous Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Squamous Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Set Ears Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Set Ears in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Serous Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Serous Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low-Renin Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low-Renin Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low T3 Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low T3 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Myofibroblastic Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Myofibroblastic Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low-Grade Fibromyxoid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low-Grade Fibromyxoid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Salivary Gland Low Grade Cribriform Cystadenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Salivary Gland Low Grade Cribriform Cystadenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Msi-Low Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Msi-Low in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vasopressin Low Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vasopressin Low in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Lymphoma (Neoplasm) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Lymphoma (Neoplasm) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade B-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade B-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Prostatic Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Prostatic Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Endometrial Stromal Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Endometrial Stromal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Low Back Pain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Astrocytoma, Low-Grade, Somatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Astrocytoma, Low-Grade, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Papillary Transitional Cell Neoplasm Of Low Malignant Potential Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Papillary Transitional Cell Neoplasm Of Low Malignant Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Dysplastic Nodule Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Dysplastic Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Ductal Breast Carcinoma In Situ Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Ductal Breast Carcinoma In Situ in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low-Grade Salivary Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low-Grade Salivary Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Central Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Central Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Cervical Squamous Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Cervical Squamous Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Frequency Deafness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Frequency Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Fibromyxoid Sarcoma With Giant Collagen Rosettes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Fibromyxoid Sarcoma With Giant Collagen Rosettes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Anterior Resection Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Anterior Resection Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormally Low-Pitched Voice Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormally Low-Pitched Voice in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Gastric Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Gastric Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Astrocytic Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Astrocytic Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Appendiceal Mucinous Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Appendiceal Mucinous Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade B-Cell Non-Hodgkin'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade B-Cell Non-Hodgkin'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Low Grade Serous Adenocarcinoma Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Low Grade Serous Adenocarcinoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Anorectal Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Anorectal Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polymorphous Low Grade Adenocarcinoma Of Salivary Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Low Grade Adenocarcinoma Of Salivary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low-Output Congestive Heart Failure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low-Output Congestive Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ulcerative Colitis-Associated Low-Grade Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ulcerative Colitis-Associated Low-Grade Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Posterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Posterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-Set, Posteriorly Rotated Ears Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-Set, Posteriorly Rotated Ears in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Very Low Birth Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Anterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Anterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prothrombin Time Low Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prothrombin Time Low in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Hanging Columella Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Hanging Columella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Infant, Extremely Low Birth Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infant, Extremely Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Pulse Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Pulse Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Alkaline Phosphatase Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Alkaline Phosphatase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Plasma Citrulline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Plasma Citrulline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Creatinine Low Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Creatinine Low in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Serum Estradiol Levels Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Serum Estradiol Levels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Self-Esteem Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Self-Esteem in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Grade Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Grade Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Iron Low (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Iron Low (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mch - Low Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mch - Low in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-Molecular-Weight Proteinuria Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-Molecular-Weight Proteinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-To-Normal Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-To-Normal Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Maternal Serum Estriol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Maternal Serum Estriol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Serum Calcitriol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Serum Calcitriol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Frustration Tolerance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Frustration Tolerance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-Set Nipples Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-Set Nipples in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Urinary Cyclic Amp Response To Pth Administration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Urinary Cyclic Amp Response To Pth Administration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Iq Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Iq in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Renal Threshold For Glucose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Renal Threshold For Glucose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormally Low T Cell Receptor Excision Circle Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormally Low T Cell Receptor Excision Circle Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Csf 5-Methyltetrahydrofolate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Csf 5-Methyltetrahydrofolate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low 1-Minute Apgar Score Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low 1-Minute Apgar Score in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Cardiac Output Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Cardiac Output in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain, Posterior Compartment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain, Posterior Compartment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain, Postural Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain, Postural in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Apgar Score Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Apgar Score in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Insertion Of Columella Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Insertion Of Columella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-Frequency Sensorineural Hearing Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-Frequency Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
low voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low-affinity IgE receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low-affinity IgE receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low-affinity IgG receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low-affinity IgG receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low-affinity glucose:sodium symporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low-affinity glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low-affinity phosphate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the low-affinity phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
low mean erythrocyte cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the low mean erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
low sweet preference Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the low sweet preference phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased CD103-positive CD11b-low dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased CD103-positive CD11b-low dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased Ly6C low monocyte number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased Ly6C low monocyte number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
low preference for an addictive substance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the low preference for an addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased CD103-positive CD11b-low dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased CD103-positive CD11b-low dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased CD11b-low dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased CD11b-low dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased Ly6C low monocyte number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased Ly6C low monocyte number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased CD11b-low dendritic cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased CD11b-low dendritic cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased Ly6C low monocyte number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased Ly6C low monocyte number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased CD11b-low dendritic cell number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased CD11b-low dendritic cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased CD11b-low dendritic cell number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased CD11b-low dendritic cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased Ly6C low monocyte number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased Ly6C low monocyte number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased CD103-positive CD11b-low dendritic cell number Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased CD103-positive CD11b-low dendritic cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Claudin-low cell_Bladder_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Claudin-low cell_Bladder_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Liver_CT2_Eomes low Liver NK cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Liver_CT2_Eomes low Liver NK cell cell type from the HuBMAP ASCT+B dataset. |
Liver_CT2_TBet low Liver NK cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Liver_CT2_TBet low Liver NK cell cell type from the HuBMAP ASCT+B dataset. |
Liver_CT2_Eomes low Liver NK cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Liver_CT2_Eomes low Liver NK cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Liver_CT2_TBet low Liver NK cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Liver_CT2_TBet low Liver NK cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
low voltage-gated calcium channel activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
low-affinity IgE receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low-affinity IgE receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
low-affinity IgG receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low-affinity IgG receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
low-affinity D-glucose:sodium symporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low-affinity D-glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
low-affinity sodium:dicarboxylate symporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
low-affinity phosphate transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the low-affinity phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Low tension glaucoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Low tension glaucoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Low grade glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Low grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Low tension glaucoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Low tension glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood low-grade glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood low-grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
T2-low asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease T2-low asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diffuse low-grade glioma, MAPK pathway–altered Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse low-grade glioma, MAPK pathway–altered in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Low compliance bladder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Low compliance bladder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polymorphous low grade neuroepithelial tumour of the young Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polymorphous low grade neuroepithelial tumour of the young in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary low grade serous adenocarcinoma of ovary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary low grade serous adenocarcinoma of ovary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Low phospholipid associated cholelithiasis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Low phospholipid associated cholelithiasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Low-set ears Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Low-set ears phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Serum C-reactive protein concentration in low fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum C-reactive protein concentration in low fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Age-related hearing impairment (low/mid frequency) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related hearing impairment (low/mid frequency) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low HDL-cholesterol levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low HDL-cholesterol levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Protein level change in low calorie diet obesity intervention Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Protein level change in low calorie diet obesity intervention phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in heavy smokers (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in heavy smokers (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in never smokers (low FEV1 vs average FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in never smokers (low FEV1 vs average FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung function in never smokers (low FEV1 vs high FEV1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung function in never smokers (low FEV1 vs high FEV1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Decreased low contrast letter acuity in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Decreased low contrast letter acuity in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low tan response Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low tan response phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Emphysema annual change measurement in smokers (percent low attenuation area) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Emphysema annual change measurement in smokers (percent low attenuation area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glaucoma (low intraocular pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glaucoma (low intraocular pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low myopia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low myopia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low myopia vs hyperopia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low myopia vs hyperopia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Survival in microsatellite instability low/stable colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Survival in microsatellite instability low/stable colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (low sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low urine pH Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low urine pH phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HIgh-sensitivity cardiac troponin T levels (high vs low) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIgh-sensitivity cardiac troponin T levels (high vs low) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Disrupted circadian rhythm (low relative amplitude of rest-activity cycles) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disrupted circadian rhythm (low relative amplitude of rest-activity cycles) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depressive symptom (low self-esteem) (ordinal trait) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depressive symptom (low self-esteem) (ordinal trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low white blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low white blood cell count (conditioned on rs2814778) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low white blood cell count (conditioned on rs2814778) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low susceptibility to hepatitis C infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low susceptibility to hepatitis C infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Low vWF levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Low vWF levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC7708794-mmc2.xlsx-DGE_table_Imm-high_vs_Imm-low-TFT_TBXT Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC7708794-mmc2.xlsx-DGE_table_Imm-high_vs_Imm-low-TFT_TBXT transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the triglyceride-rich lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
plasma lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
plasma lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plasma lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the triglyceride-rich lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
FSL-1 lipoprotein, synthetic Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical FSL-1 lipoprotein, synthetic from the curated CTD Gene-Chemical Interactions dataset. |
Lipoprotein Glomerulopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipoprotein Glomerulopathy from the curated CTD Gene-Disease Associations dataset. |
lipoprotein A-I [Supplementary Concept] Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait lipoprotein A-I [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Lipoprotein(a) Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Lipoprotein(a) in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
familial lipoprotein lipase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial lipoprotein lipase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
OspA lipoprotein Gene Setinteracting proteins for the OspA lipoprotein drug from the curated DrugBank Drug Targets dataset. |
cholesterol, hdl; lipoprotein, ldl Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; lipoprotein, ldl in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein distribution of apoc-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein distribution of apoc-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein(a) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein(a) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; lipoprotein; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; lipoprotein; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery reactivity; lipoprotein oxidation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery reactivity; lipoprotein oxidation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; diabetes, type 2; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; diabetes, type 2; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; triglycerides; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; triglycerides; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
differential plasma lipoprotein response to simvastatin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease differential plasma lipoprotein response to simvastatin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; triglycerides; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; triglycerides; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein (a) concentration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein (a) concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; lipoprotein; cerebral infarct Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; lipoprotein; cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein(a) concentration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein(a) concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypolipoproteinemias; lipoprotein; deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypolipoproteinemias; lipoprotein; deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; lipoprotein, ldl; atherosclerosis, coronary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; lipoprotein, ldl; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lower lipoprotein lipase activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lower lipoprotein lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein a-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein a-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein; antiphospholipid syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein; antiphospholipid syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipoprotein(a) levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipoprotein(a) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; lipoprotein; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; lipoprotein; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein, ldl Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein, ldl in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; lipoprotein; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; lipoprotein; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein, ldl; cholesterol, ldl Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein, ldl; cholesterol, ldl in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein level Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; lipoprotein; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; lipoprotein; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein subclass profiles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein subclass profiles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anti-atherogenic lipoprotein profile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anti-atherogenic lipoprotein profile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; diabetes, type 2; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; diabetes, type 2; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein; fatty acid; uric acid Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein; fatty acid; uric acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein, ldl; lipids; preeclampsia; apolipoproteins Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein, ldl; lipids; preeclampsia; apolipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; cholesterol, total; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; cholesterol, total; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; atherosclerosis, coronary; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; atherosclerosis, coronary; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein glomerulopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipoprotein glomerulopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipoprotein traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; lipoprotein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipoprotein Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lipoprotein in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
negative regulation of lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein particle mediated signaling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein particle mediated signaling biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma lipoprotein particle assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein modification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein modification biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of plasma lipoprotein particle oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein localization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein localization biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of plasma lipoprotein particle levels Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of plasma lipoprotein particle levels biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma lipoprotein particle organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the triglyceride-rich lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of plasma lipoprotein particle oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to lipoprotein particle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to lipoprotein particle biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to lipoprotein particle stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the triglyceride-rich lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
lipoprotein particle receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipoprotein transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipoprotein lipase activator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein lipase activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipoprotein lipase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipoprotein lipase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Lipoprotein lipase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipoprotein lipase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased lipoprotein lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lipoprotein lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipoprotein lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lipoprotein lipase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the lipoprotein lipase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
lipoprotein glomerulopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the lipoprotein glomerulopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
Lipoprotein metabolism Gene Setproteins participating in the Lipoprotein metabolism pathway from the Reactome Pathways dataset. |
Familial Lipoprotein Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Lipoprotein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipoprotein Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipoprotein Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipoprotein Glomerulopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipoprotein Glomerulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipoprotein (A) Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lipoprotein (A) Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lipoprotein Lipase (Olbia) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lipoprotein Lipase (Olbia) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
detection of bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of plasma lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of plasma lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
plasma lipoprotein particle oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein localization to membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein localization to membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein localization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein localization biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of plasma lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of plasma lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
lipoprotein lipase activator activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipoprotein lipase activator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
lipoprotein lipase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipoprotein lipase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
increased lipoprotein lipase activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lipoprotein lipase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lipoprotein lipase activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lipoprotein lipase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Plasma lipoprotein assembly Gene Setproteins participating in the Plasma lipoprotein assembly pathway from the Reactome Pathways 2024 dataset. |
Plasma lipoprotein clearance Gene Setproteins participating in the Plasma lipoprotein clearance pathway from the Reactome Pathways 2024 dataset. |
Plasma lipoprotein remodeling Gene Setproteins participating in the Plasma lipoprotein remodeling pathway from the Reactome Pathways 2024 dataset. |
detection of bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipoprotein transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipoprotein transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of plasma lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of plasma lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipoprotein lipase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
plasma lipoprotein particle oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein localization to membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein localization to membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein localization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein localization biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipoprotein transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipoprotein transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to bacterial lipoprotein Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to bacterial lipoprotein biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of plasma lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of plasma lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipoprotein metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipoprotein metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
lipoprotein lipase activator activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipoprotein lipase activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
lipoprotein lipase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipoprotein lipase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
lipoprotein particle binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
lipoprotein particle receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Familial lipoprotein lipase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial lipoprotein lipase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Plasma lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Plasma lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Plasma lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the triglyceride-rich plasma lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
LIPOPROTEIN LIPASE Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the LIPOPROTEIN LIPASE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lipoprotein glomerulopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lipoprotein glomerulopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lipoprotein Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lipoprotein phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lipoprotein (a) levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein (a) levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein(a) levels adjusted for apolipoprotein(a) isoforms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein(a) levels adjusted for apolipoprotein(a) isoforms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein (a) levels in response to niacin in statin-treated individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein (a) levels in response to niacin in statin-treated individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein (a) levels in coronary artery disease (percutaneous coronary intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein (a) levels in coronary artery disease (percutaneous coronary intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein (a) - cholesterol levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein (a) - cholesterol levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid or lipoprotein levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid or lipoprotein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein phospholipase A2 activity in cardiovascular disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein phospholipase A2 activity in cardiovascular disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
OSPA LIPOPROTEIN Gene Setinteracting proteins for the OSPA LIPOPROTEIN drug from theDGIdb Drug Targets 2026 dataset. |
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
anxiety and hostility and depression Gene SetFrom 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 SetFrom 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 SetFrom 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. |
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene SetFrom 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 SetFrom 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 SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins 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 Setproteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF and miRs in smooth muscle differentiation and proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE and miR 146 in inflammation and atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH and its relationship to dietary restriction and aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins 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 2024 dataset. |
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Setproteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset. |
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Setproteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Setproteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Setproteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Basic cell groups and regions Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset. |
corticosteroids and cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity and toxicity Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing and presentation Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development and pigmentation pathway Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis and proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom 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. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom 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. |
Cutis Gyrata syndrome of Beare and Stevenson Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- and BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage and polyadenylation factor (CPSF) Gene Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, and Proteins Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom 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. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset. |
Hypopituitarism and septooptic 'dysplasia' Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset. |
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal and Salivary Glands Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Calcification of Joints and Arteries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset. |
CHOANAL ATRESIA AND LYMPHEDEMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy, Type IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset. |
Asthma, Nasal Polyps, And Aspirin Intolerance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Germ Cell and Embryonal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset. |
Cutis Gyrata Syndrome of Beare And Stevenson Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Wounds and Injuries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset. |
Schizophrenia and Disorders with Psychotic Features Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset. |
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Sleep Initiation and Maintenance Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset. |
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Generalized Epilepsy and Paroxysmal Dyskinesia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast and Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Keratosis palmoplantaris with periodontopathia and onychogryposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia and onychogryposis from the curated CTD Gene-Disease Associations dataset. |
Intracranial Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Nevi and Melanomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nevi and Melanomas from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Attention Deficit and Disruptive Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy dilated with Woolly hair and keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset. |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset. |
Mullerian Aplasia and Hyperandrogenism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
Esophageal and Gastric Varices Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal and Gastric Varices from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset. |
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, squamous cell of head and neck Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head and neck from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
Extravasation of Diagnostic and Therapeutic Materials Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic and Therapeutic Materials from the curated CTD Gene-Disease Associations dataset. |
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Knuckle pads, leuconychia and sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia and sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hyperekplexia and Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia and glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset. |
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Sarcoma family syndrome of Li and Fraumeni Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset. |
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset. |
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa and Deafness from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset. |
Lipoid Proteinosis of Urbach and Wiethe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach and Wiethe from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset. |