Name

abnormality of the basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Abnormality Of The Basal Ganglia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

central subpallium (classic basal ganglia) Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in central subpallium (classic basal ganglia) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basal ganglia calcification, idiopathic, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Basal ganglia calcification, idiopathic, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Idiopathic basal ganglia calcification 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Idiopathic basal ganglia calcification 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Idiopathic basal ganglia calcification 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Idiopathic basal ganglia calcification 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Basal ganglia disease, biotin-responsive from the curated CTD Gene-Disease Associations dataset.

Basal Ganglia Diseases Gene Set

From CTD Gene-Disease Associations

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

Idiopathic basal ganglia calcification 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Idiopathic basal ganglia calcification 1 from the curated CTD Gene-Disease Associations dataset.

basal ganglia disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

biotin-responsive basal ganglia disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease biotin-responsive basal ganglia disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

basal ganglia disease Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

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

biotin-responsive basal ganglia disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

basal ganglia disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

basal ganglia diseases; Gene Set

From GAD Gene-Disease Associations

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

basal ganglia diseases Gene Set

From GAD Gene-Disease Associations

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

basal ganglia diseases; dyskinesia, drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal ganglia diseases; dyskinesia, drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; basal ganglia diseases Gene Set

From GAD Gene-Disease Associations

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

gabaergic neuron differentiation in basal ganglia Gene Set

From GO Biological Process Annotations 2015

genes participating in the gabaergic neuron differentiation in basal ganglia biological process from the curated GO Biological Process Annotations 2015 dataset.

basal ganglia disease Gene Set

From GWASdb SNP-Disease Associations

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

focal t2 hyperintense basal ganglia lesion Gene Set

From HPO Gene-Disease Associations

genes associated with the focal t2 hyperintense basal ganglia lesion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

basal ganglia gliosis Gene Set

From HPO Gene-Disease Associations

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

neuronal loss in basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cavitation of the basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the cavitation of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

basal ganglia calcification Gene Set

From HPO Gene-Disease Associations

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

basal ganglia cysts Gene Set

From HPO Gene-Disease Associations

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

abnormal basal ganglia mri signal intensity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bilateral basal ganglia lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral basal ganglia lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetric lesions of the basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetric lesions of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large basal ganglia Gene Set

From HPO Gene-Disease Associations

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

Basal Ganglia Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Basal Ganglia Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

loss of basal ganglia neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

basal ganglia calcification, idiopathic, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal ganglia calcification, idiopathic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

basal ganglia calcification, idiopathic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal ganglia calcification, idiopathic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

basal ganglia calcification, idiopathic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal ganglia calcification, idiopathic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

basal ganglia calcification, idiopathic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal ganglia calcification, idiopathic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Basal Ganglia Cysts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Ganglia Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Idiopathic Basal Ganglia Calcification 1 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Idiopathic Basal Ganglia Calcification 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cavitation Of The Basal Ganglia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cavitation Of The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symmetric Lesions Of The Basal Ganglia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Symmetric Lesions Of The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Ganglia Calcification Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Ganglia Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lesions In The Basal Ganglia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lesions In The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Ganglia Disease, Biotin-Responsive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Ganglia Disease, Biotin-Responsive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Dysgenesis Of The Basal Ganglia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Dysgenesis Of The Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Ganglia Gliosis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Basal Ganglia Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Small Basal Ganglia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Small Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Large Basal Ganglia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Large Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Basal Ganglia Mri Signal Intensity Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Basal Ganglia Mri Signal Intensity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Focal T2 Hyperintense Basal Ganglia Lesion Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Focal T2 Hyperintense Basal Ganglia Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Basal Ganglia Calcification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Basal Ganglia Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Focal T2 Hypointense Basal Ganglia Lesion Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Focal T2 Hypointense Basal Ganglia Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Bilateral Basal Ganglia Lesions Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bilateral Basal Ganglia Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Neuronal Loss In Basal Ganglia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neuronal Loss In Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

T2 Hypointense Basal Ganglia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype T2 Hypointense Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

loss of basal ganglia neurons Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Brain - Nucleus accumbens (basal ganglia) Gene Set

From GTEx Tissue Gene Expression Profiles 2023

genes with high or low expression in Brain - Nucleus accumbens (basal ganglia) relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.

Brain - Putamen (basal ganglia) Gene Set

From GTEx Tissue Gene Expression Profiles 2023

genes with high or low expression in Brain - Putamen (basal ganglia) relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.

Brain - Caudate (basal ganglia) Gene Set

From GTEx Tissue Gene Expression Profiles 2023

genes with high or low expression in Brain - Caudate (basal ganglia) relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.

Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) Gene Set

From Reactome Pathways 2024

proteins participating in the Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) pathway from the Reactome Pathways 2024 dataset.

Basal ganglia disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Basal ganglia disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

biotin-responsive basal ganglia disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease biotin-responsive basal ganglia disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Basal ganglia calcification Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Basal ganglia calcification in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Basal ganglia disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Basal ganglia disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

biotin-responsive basal ganglia disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease biotin-responsive basal ganglia disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Basal ganglia cerebrovascular disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Basal ganglia cerebrovascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Biotin-responsive basal ganglia disease Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Biotin-responsive basal ganglia disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Idiopathic basal ganglia calcification Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Idiopathic basal ganglia calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Basal ganglia calcification Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Basal ganglia calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Focal T2 hyperintense basal ganglia lesion Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Focal T2 hyperintense basal ganglia lesion phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Basal ganglia growth Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Basal ganglia growth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

abnormality of the enteric ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the enteric ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; skin basal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

ganglia Gene Set

From GeneRIF Biological Term Annotations

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

Brn3a_KO_GDS1651_248_mouse_Embryonic (day 13.5) trigeminal ganglia - homozygous Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Brn3a_KO_GDS1651_248_mouse_Embryonic (day 13.5) trigeminal ganglia - homozygous gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

Brn3a_KO_GDS1651_247_mouse_Embryonic (day 13.5) trigeminal ganglia - heterozygous Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Brn3a_KO_GDS1651_247_mouse_Embryonic (day 13.5) trigeminal ganglia - heterozygous gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

paravertebral ganglia hyperplasia Gene Set

From MPO Gene-Phenotype Associations

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

prevertebral ganglia hyperplasia Gene Set

From MPO Gene-Phenotype Associations

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

abnormal enteric ganglia morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cranial ganglia morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cranial ganglia morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal cranial ganglia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal enteric ganglia morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal enteric ganglia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

paravertebral ganglia hyperplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the paravertebral ganglia hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

prevertebral ganglia hyperplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the prevertebral ganglia hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small prevertebral sympathetic ganglia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small prevertebral sympathetic ganglia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

basal nucleus of meynert, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basal nucleus of meynert, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

basal reticular formation of p1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal reticular formation of p1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal part of terminal hypothalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal part of terminal hypothalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

medial basal reticular formation of m1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in medial basal reticular formation of m1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r10 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r10 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal plate of p1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal plate of p1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal plate of p3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal plate of p3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal plate of p2 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal plate of p2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r8 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r8 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r3 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r3 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal plate of m1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal plate of m1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lower basal perifornical nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lower basal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

reticular formation of basal m2 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in reticular formation of basal m2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal peduncular hypothalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basal peduncular hypothalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r4 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r4 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

isthmic basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in isthmic basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r2 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r2 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r5 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r5 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper basal perifornical nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in upper basal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lower basal lateral hypothalamic area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lower basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r7 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r7 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

m2 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in m2 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

substantia innominata/basal nucleus, transitional part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in substantia innominata/basal nucleus, transitional part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r9 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r9 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

substantia innominata/basal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in substantia innominata/basal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r6 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r6 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r1 basal plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r1 basal plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper basal lateral hypothalamic area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in upper basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basal nucleus of Meynert Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basal nucleus of Meynert relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

basolateral nucleus (basal nucleus) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basolateral nucleus (basal nucleus) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

basomedial nucleus (accessory basal nucleus) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basomedial nucleus (accessory basal nucleus) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

basal ventral medial nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in basal ventral medial nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Basal laminar drusen Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Basal laminar drusen phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

basal cortex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basal cortex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basal plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basal plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basal lamina Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basal lamina cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ciliary basal body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ciliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basal part of cell Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basal part of cell cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basal cortex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

basal plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

basal lamina Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

bacterial-type flagellum basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the bacterial-type flagellum basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basal pole of neuron Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the basal pole of neuron cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basal labyrinth Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

ciliary basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ciliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basal part of cell Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the basal part of cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Basal Cell Nevus Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Basal Cell Nevus Syndrome from the curated CTD Gene-Disease Associations dataset.

Carcinoma, Basal Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoma, Basal Cell from the curated CTD Gene-Disease Associations dataset.

Basal Laminar Drusen Gene Set

From CTD Gene-Disease Associations

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

Carcinoma, Basal Cell Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Carcinoma, Basal Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

nevoid basal cell carcinoma syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease nevoid basal cell carcinoma syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

infiltrative basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

sarcomatoid basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

nodular basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

morpheaform basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

nevoid basal cell carcinoma syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease nevoid basal cell carcinoma syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

signet ring basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease signet ring basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

superficial basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

pigmented basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

fibroepithelial basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

adenoid basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

vulva basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

clear cell basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

infundibulocystic basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

plasma glucose, basal hepatic glucose and increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

cerebellar medulloblastomas and cutaneous basal cell carcinomas. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar medulloblastomas and cutaneous basal cell carcinomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal metabolism Gene Set

From GAD Gene-Disease Associations

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

skin cancer; squamous cell carcinoma; carcinoma, basal cell Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

neoplasms, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; carcinoma, basal cell; carcinoma, ductal, breast Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma, basal cell; carcinoma, ductal, breast in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

nevoid basal cell carcinoma syndrome associated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nevoid basal cell carcinoma syndrome associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

basal cell carcinoma (cutaneous) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal cell carcinoma (cutaneous) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

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

testosterone; fsh, basal; inhibin b levels; semen parameters Gene Set

From GAD Gene-Disease Associations

genes associated with the disease testosterone; fsh, basal; inhibin b levels; semen parameters in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal Gene Set

From GeneRIF Biological Term Annotations

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

basal protein localization Gene Set

From GO Biological Process Annotations 2015

genes participating in the basal protein localization biological process from the curated GO Biological Process Annotations 2015 dataset.

maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

squamous basal epithelial stem cell differentiation involved in prostate gland acinus development Gene Set

From GO Biological Process Annotations 2015

genes participating in the squamous basal epithelial stem cell differentiation involved in prostate gland acinus development biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment or maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment or maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

ciliary basal body organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the ciliary basal body organization biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment or maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment or maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2015 dataset.

basal cortex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the basal cortex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

basal plasma membrane Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the basal plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.

axonemal basal plate Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the axonemal basal plate cellular component from the curated GO Cellular Component Annotations 2015 dataset.

basal lamina Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the basal lamina cellular component from the curated GO Cellular Component Annotations 2015 dataset.

basal part of cell Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the basal part of cell cellular component from the curated GO Cellular Component Annotations 2015 dataset.

ciliary basal body Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the ciliary basal body cellular component from the curated GO Cellular Component Annotations 2015 dataset.

rna polymerase ii basal transcription factor binding transcription factor activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the rna polymerase ii basal transcription factor binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

rna polymerase ii basal transcription factor binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the rna polymerase ii basal transcription factor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

basal rna polymerase ii transcription machinery binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the basal rna polymerase ii transcription machinery binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

basal transcription machinery binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the basal transcription machinery binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

Basal cell carcinoma Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Basal cell carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

basal cell carcinoma Gene Set

From GWASdb SNP-Disease Associations

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

pigmented basal cell carcinoma Gene Set

From GWASdb SNP-Disease Associations

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

basal cell carcinoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the basal cell carcinoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

basal cell carcinoma Gene Set

From HPO Gene-Disease Associations

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

anterior basal encephalocele Gene Set

From HPO Gene-Disease Associations

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

basal lamina 'onion bulb' formation Gene Set

From HPO Gene-Disease Associations

genes associated with the basal lamina 'onion bulb' formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Basal Cell Nevus Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Basal Cell Nevus Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Basal Cell Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Basal Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Carcinoma, Basal Cell Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Carcinoma, Basal Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Basal body-orientation factor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Basal body-orientation factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

basal cell carcinoma Gene Set

From KEGG Pathways

proteins participating in the basal cell carcinoma pathway from the KEGG Pathways dataset.

basal transcription factors Gene Set

From KEGG Pathways

proteins participating in the basal transcription factors pathway from the KEGG Pathways dataset.

abnormal basal lamina morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal basal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent strial basal cell tight junctions Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent strial basal cell tight junctions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal airway basal cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal airway basal cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased basal metabolism Gene Set

From MPO Gene-Phenotype Associations

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

abnormal airway basal cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased basal cell carcinoma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased basal cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basal metabolism Gene Set

From MPO Gene-Phenotype Associations

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

airway basal cell hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the airway basal cell hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal strial basal cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

{basal cell carcinoma, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

basal laminar drusen Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal laminar drusen phenotype from the curated OMIM Gene-Disease Associations dataset.

basal cell nevus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal cell nevus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

basal cell carcinoma, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the basal cell carcinoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{basal cell carcinoma, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {basal cell carcinoma, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

Anchoring of the basal body to the plasma membrane Gene Set

From Reactome Pathways 2014

proteins participating in the Anchoring of the basal body to the plasma membrane pathway from the Reactome Pathways dataset.

basal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

basal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

basal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

meynert's basal nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue meynert's basal nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

basal cell carcinoma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

basal telencephalon Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

basal forebrain Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

basal cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Lung-basal cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Lung-basal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Mammary-basal cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Mammary-basal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Prostate-basal cell of prostate epithelium Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Prostate-basal cell of prostate epithelium relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Salivary_Gland-basal cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Salivary_Gland-basal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Tongue-basal cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Tongue-basal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Trachea-basal cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Trachea-basal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Basal-Like Breast Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal-Like Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Carcinoma, Basal Cell Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Carcinoma, Basal Cell in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Follicular Atrophoderma And Basal Cell Epitheliomata Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Follicular Atrophoderma And Basal Cell Epitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Nevus Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Nevus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Anterior Basal Encephalocele Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Anterior Basal Encephalocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Encephalocele Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Encephalocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Laminar Drusen (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Laminar Drusen (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pigmented Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pigmented Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Cancer Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Neoplasm Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Irritated Basal Cell Papilloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Irritated Basal Cell Papilloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Superficial Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Superficial Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Metastatic Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Metastatic Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Ganglion Degeneration Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Ganglion Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Adenocarcinoma Of Salivary Gland Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Adenocarcinoma Of Salivary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Basal Cell Papillomata Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Basal Cell Papillomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Prostate Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Prostate Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Epidermolysis Bullosa Simplex Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Epidermolysis Bullosa Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Skin Nodular Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Skin Nodular Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Basal Cell Nevus Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Basal Cell Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Malignant Basal Cell Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Malignant Basal Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Experimental Organism Basal Cell Carcinoma Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Experimental Organism Basal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Basal Lamina Onion Bulb Formation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Basal Lamina Onion Bulb Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

establishment of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

basal dendrite development Gene Set

From GO Biological Process Annotations 2023

genes participating in the basal dendrite development biological process from the curated GO Biological Process Annotations 2023 dataset.

basal dendrite arborization Gene Set

From GO Biological Process Annotations 2023

genes participating in the basal dendrite arborization biological process from the curated GO Biological Process Annotations 2023 dataset.

ciliary basal body organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the ciliary basal body organization biological process from the curated GO Biological Process Annotations 2023 dataset.

squamous basal epithelial stem cell differentiation involved in prostate gland acinus development Gene Set

From GO Biological Process Annotations 2023

genes participating in the squamous basal epithelial stem cell differentiation involved in prostate gland acinus development biological process from the curated GO Biological Process Annotations 2023 dataset.

establishment or maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment or maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

establishment of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

ciliary basal body-plasma membrane docking Gene Set

From GO Biological Process Annotations 2023

genes participating in the ciliary basal body-plasma membrane docking biological process from the curated GO Biological Process Annotations 2023 dataset.

basal protein localization Gene Set

From GO Biological Process Annotations 2023

genes participating in the basal protein localization biological process from the curated GO Biological Process Annotations 2023 dataset.

basal dendrite morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the basal dendrite morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

establishment or maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment or maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2023 dataset.

basal dendrite Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the basal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset.

basal ectoplasmic specialization Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the basal ectoplasmic specialization cellular component from the curated GO Cellular Component Annotations 2023 dataset.

kinociliary basal body Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the kinociliary basal body cellular component from the curated GO Cellular Component Annotations 2023 dataset.

basal RNA polymerase II transcription machinery binding Gene Set

From GO Molecular Function Annotations 2023

genes performing the basal RNA polymerase II transcription machinery binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

abnormal horizontal basal cell of olfactory epithelium morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal horizontal basal cell of olfactory epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal basal ganglion morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal basal ganglion morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased basal metabolism Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased basal metabolism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent strial basal cell tight junctions Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent strial basal cell tight junctions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal basal lamina morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal basal lamina morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal basal metabolism Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal basal metabolism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal strial basal cell morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal strial basal cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased basal cell carcinoma incidence Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased basal cell carcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased basal metabolism Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased basal metabolism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal airway basal cell differentiation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal airway basal cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

airway basal cell hyperplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the airway basal cell hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

basal brain tissue herniation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the basal brain tissue herniation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Human - Lung v1 - L1 - Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v1 - L1 - Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v1 - L2 - Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v1 - L2 - Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v1 - L2 - Proliferating Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v1 - L2 - Proliferating Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v1 - L2 - Differentiating Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v1 - L2 - Differentiating Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v1 - L2 - Proximal Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v1 - L2 - Proximal Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v2 (HLCA) - L3 - Basal Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v2 (HLCA) - L3 - Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v2 (HLCA) - L4 - Basal resting Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v2 (HLCA) - L4 - Basal resting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Lung v2 (HLCA) - Finest - Basal resting Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Lung v2 (HLCA) - Finest - Basal resting cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Tonsil - L2 - Basal cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Tonsil - L2 - Basal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Basal cell_Distal airway_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Distal airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Bladder_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Bladder_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Bone marrow_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Horizontal basal cell_Brain_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Horizontal basal cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal progenitor cell_Breast_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal progenitor cell_Breast_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Breast_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Breast_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Breast_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Breast_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Breast_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Breast_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Mammary gland_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Mammary gland_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Epithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Cochlea_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Cochlea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial progenitor cell_Endometrium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial progenitor cell_Endometrium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Airway epithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Airway epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Esophagus_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal progenitor cell_Esophagus_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal progenitor cell_Esophagus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Esophagus_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Esophagus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Transitional basal progenitor cell_Esophagus_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Transitional basal progenitor cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Esophagus_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Eye_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Eye_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Liver_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Lung_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Bronchus_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Bronchus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal-like cell_Lung_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal-like cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Airway_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Lung_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Bronchiole_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Bronchiole_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Mammary gland_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Mammary gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Procr+ basal cell_Mammary gland_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Procr+ basal cell_Mammary gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Respiratory horizontal basal cell_Olfactory neuroepithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Respiratory horizontal basal cell_Olfactory neuroepithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Olfactory neuroepithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Olfactory neuroepithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Horizontal basal cell_Olfactory neuroepithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Horizontal basal cell_Olfactory neuroepithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Globose basal cell_Olfactory neuroepithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Globose basal cell_Olfactory neuroepithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Buccal mucosal epithelium_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Buccal mucosal epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal-like cell_Pancreas_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal-like cell_Pancreas_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Pancreas_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Pancreas_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Prostate_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Prostate_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Prostate_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Epidermis_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Epidermis_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal outer layer cell_Skin_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal outer layer cell_Skin_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal keratinocyte_Skin_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal keratinocyte_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Skin_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal forebrain cholinergic neuron (BFCN)_Skin_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal forebrain cholinergic neuron (BFCN)_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal epithelial cell_Skin_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal epithelial cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Differentiated interfollicular epidermis basal cell_Interfollicular epidermis_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Differentiated interfollicular epidermis basal cell_Interfollicular epidermis_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Infundibulum basal layer cell_Hair follicle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Infundibulum basal layer cell_Hair follicle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Infundibulum basal layer cell_Interfollicular epidermis_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Infundibulum basal layer cell_Interfollicular epidermis_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Undifferentiated interfollicular epidermis basal cell_Interfollicular epidermis_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Undifferentiated interfollicular epidermis basal cell_Interfollicular epidermis_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal gland mucous cell_Stomach_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal gland mucous cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Trachea_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Trachea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Cycling basal cell_Trachea_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Cycling basal cell_Trachea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Airway basal cell_Trachea_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Airway basal cell_Trachea_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Undefined_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Basal cell_Epithelium_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Basal cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Anchoring of the basal body to the plasma membrane Gene Set

From Reactome Pathways 2024

proteins participating in the Anchoring of the basal body to the plasma membrane pathway from the Reactome Pathways 2024 dataset.

Respiratory system_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Annotations

biomarker genes for the Respiratory system_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset.

Trachea_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Annotations

biomarker genes for the Trachea_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset.

Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Annotations

biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset.

Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.

Respiratory system_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

biomarker genes for the Respiratory system_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.

Trachea_CT1_airway submucosal gland duct basal cell Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

biomarker genes for the Trachea_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.

establishment of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

basal dendrite development Gene Set

From GO Biological Process Annotations 2025

genes participating in the basal dendrite development biological process from the curated GO Biological Process Annotations 2025 dataset.

basal dendrite arborization Gene Set

From GO Biological Process Annotations 2025

genes participating in the basal dendrite arborization biological process from the curated GO Biological Process Annotations 2025 dataset.

ciliary basal body organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the ciliary basal body organization biological process from the curated GO Biological Process Annotations 2025 dataset.

squamous basal epithelial stem cell differentiation involved in prostate gland acinus development Gene Set

From GO Biological Process Annotations 2025

genes participating in the squamous basal epithelial stem cell differentiation involved in prostate gland acinus development biological process from the curated GO Biological Process Annotations 2025 dataset.

establishment or maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment or maintenance of epithelial cell apical/basal polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

establishment of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

ciliary basal body-plasma membrane docking Gene Set

From GO Biological Process Annotations 2025

genes participating in the ciliary basal body-plasma membrane docking biological process from the curated GO Biological Process Annotations 2025 dataset.

basal protein localization Gene Set

From GO Biological Process Annotations 2025

genes participating in the basal protein localization biological process from the curated GO Biological Process Annotations 2025 dataset.

basal dendrite morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the basal dendrite morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

establishment or maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment or maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the maintenance of apical/basal cell polarity biological process from the curated GO Biological Process Annotations 2025 dataset.

basal dendrite Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the basal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset.

basal ectoplasmic specialization Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the basal ectoplasmic specialization cellular component from the curated GO Cellular Component Annotations 2025 dataset.

kinociliary basal body Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the kinociliary basal body cellular component from the curated GO Cellular Component Annotations 2025 dataset.

basal RNA polymerase II transcription machinery binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the basal RNA polymerase II transcription machinery binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Basal cell carcinoma Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Basal cell carcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Nevoid basal cell carcinoma syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Nevoid basal cell carcinoma syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Basal cell carcinoma Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Basal cell carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Nevoid basal cell carcinoma syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Nevoid basal cell carcinoma syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Superficial basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Superficial basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Nodular basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Nodular basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Infiltrative basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Infiltrative basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Basal laminar drusen Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Basal laminar drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Fibroepithelial basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Fibroepithelial basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Micronodular basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Micronodular basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Pigmented basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Pigmented basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Infundibulocystic basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Infundibulocystic basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cystic basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cystic basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Adenoid basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Adenoid basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Clear cell basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Clear cell basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Morpheaform basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Morpheaform basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Anal margin basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Anal margin basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Sarcomatoid basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Sarcomatoid basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Follicular basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Follicular basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Signet ring basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Signet ring basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vulva basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vulva basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Metatypical basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Metatypical basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

External ear basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease External ear basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cervical adenoid basal carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cervical adenoid basal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Penis basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Penis basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Scrotum basal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Scrotum basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Basal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Basal ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Basal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Basal ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Basal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal forebrain Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal forebrain in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Meynert's basal nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Meynert's basal nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal swimming muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal swimming muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal telencephalon Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal telencephalon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal node Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal cell carcinoma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal cell carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Basal prostate epithelium cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Basal prostate epithelium cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Ciliary basal body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Ciliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basal part of cell Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Basal part of cell cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basal plasma membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Basal plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basal cortex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Basal cortex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Kinociliary basal body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Kinociliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Axonemal basal plate Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Axonemal basal plate cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basal dendrite Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Basal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basal ectoplasmic specialization Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal ectoplasmic specialization cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal cortex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal cortex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal dendrite Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal plasma membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Axonemal basal plate Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Axonemal basal plate cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal part of cell Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal part of cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Ciliary basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Ciliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal body patch Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal body patch cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal tubulobulbar complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal tubulobulbar complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal pole of outer hair cell Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal pole of outer hair cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Kinociliary basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Kinociliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

bacterial-type flagellum basal body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the bacterial-type flagellum basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

bacterial-type flagellum basal body, rod Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the bacterial-type flagellum basal body, rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal distal dendrite Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal pole of neuron Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal pole of neuron cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal labyrinth Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal labyrinth cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal proximal dendrite Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basal proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

bacterial-type flagellum basal body, distal rod, L ring Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the bacterial-type flagellum basal body, distal rod, L ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

bacterial-type flagellum basal body, distal rod Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the bacterial-type flagellum basal body, distal rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basal cell nevus syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Basal cell nevus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Basal cell carcinoma Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Basal cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Basal laminar drusen Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Basal laminar drusen phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Basal metabolic rate Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Basal metabolic rate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Basal cell carcinoma Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Basal cell carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Basal metabolic rate variance Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Basal metabolic rate variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Basal transcription factors Gene Set

From KEGG Pathways 2026

proteins participating in the Basal transcription factors pathway from the KEGG Pathways 2026 dataset.

Basal cell carcinoma Gene Set

From KEGG Pathways 2026

proteins participating in the Basal cell carcinoma pathway from the KEGG Pathways 2026 dataset.

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

From CTD Gene-Disease Associations

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

Hypertelorism with esophageal abnormality and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.

congenital nervous system abnormality Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

congenital nervous system abnormality Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

abnormality of glucagon secretion Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

gastrin secretion abnormality Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms Gene Set

From GAD Gene-Disease Associations

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

cadasil; chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

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

torsion abnormality; vascular malformations Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

smooth pursuit eye movement abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of vitamin metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of movement Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the endometrium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thyroid morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of forearm bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the integument Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin d metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of myeloid leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of divalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the stomach Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of central motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycolipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of connective tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the aortic valve Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cellular immune system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of immune serum protein physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of oral mucosa Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urethra Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of brain morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the endocrine system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the breast Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the autonomic nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pharynx Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

eeg abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femur Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the immune system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin a metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the calf Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of potassium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the carotid arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the kidney Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circle of willis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hand Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pituitary gland Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the myocardium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the biliary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cell cycle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of von willebrand factor Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of finger Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lower limb Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of long bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thrombocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of neutrophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hip bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the iris Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lower urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thyroid physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

mesangial abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin b metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating fibrinogen Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the adrenal glands Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of phalanx of finger Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the musculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the duodenum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skull base Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the astrocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urinary system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of basophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the face Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the male genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of facial skeleton Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gingiva Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the large intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lung Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating hormone level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the placenta Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ankles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral neck Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the heart valves Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of aromatic amino acid family metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prenatal development or birth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eye movement Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper limb Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ovary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the prostate Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of digit Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the testis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dental eruption Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the clavicle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the knees Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the coronary arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cardiovascular system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pleura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of interleukin secretion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of transition element cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of tryptophan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the head Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of head or neck Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the mandible Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional respiratory abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of humoral immunity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neurodevelopmental abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of taste sensation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of renin-angiotensin system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pancreas physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of primary teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the thorax Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the thyroid gland Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the abdomen Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebrospinal fluid Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the menstrual cycle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

behavioral abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the oral cavity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cholesterol metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of granulocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of monovalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the fundus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of forebrain morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the tongue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of acid-base homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vertebrae Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of iron homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of refraction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dna repair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nose Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nitrogen compound homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of central nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of erythrocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of liposaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral neck or head region Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urinary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vasculature of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the glomerulus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of unsaturated fatty acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating protein level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of copper homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

prenatal maternal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the humeral diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

phenotypic abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uterus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of female internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the metaphyses Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the common coagulation pathway Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hypothalamus-pituitary axis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fatty-acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the genitourinary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cytokine secretion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

growth abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the choroid Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the globe Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of radial diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of sodium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cells of the monocyte/macrophage lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb joint Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uvea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

biliary tract abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the abdominal organs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the esophagus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the retina Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the penis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the radius Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of urine homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the costochondral junction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

venous abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of extrapyramidal motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone marrow cell morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the liver Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of proteoglycan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fluid regulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb metaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pylorus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of adipose tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nasopharynx Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intervertebral disk Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the stapes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gallbladder Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the coagulation cascade Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the left ventricle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of zinc homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pelvic girdle bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of b cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the left ventricular outflow tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the glial cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dental structure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper arm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ulna Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral head Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal endothelium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lymphocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the mouth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vitamin b12 metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of magnesium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the small intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the genital system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the aorta Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the female genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the humerus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiovascular system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of complement system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cells of the erythroid lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

chorioretinal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of sulfur amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating cortisol level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prothrombin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of coagulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cervical spine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skull Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carboxylic acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pancreas Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skeletal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lens Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of b cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body weight Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of temperature regulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the systemic arterial tree Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the rib cage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin e metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of ion homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of macrophages Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of calcium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body height Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of polysaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intrinsic pathway Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eosinophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the macula Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of epidermal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of higher mental function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ribs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nucleobase metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the forearm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of purine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of serum cytokine level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of immune system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating leptin level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nephron Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating glucocorticoid level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the level of lipoprotein cholesterol Gene Set

From 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 neck Gene Set

From HPO Gene-Disease Associations

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

abnormality of the falx cerebri Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of myeloid leukocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of gastrointestinal vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the extraocular muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the choanae Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycolipid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal cavity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the immune system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of reticulocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cochlea Gene Set

From HPO Gene-Disease Associations

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

abnormality of von willebrand factor Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the intestine Gene Set

From HPO Gene-Disease Associations

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

abnormality of the gingiva Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lung Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the gastrointestinal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vena cava Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of sharpey fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thorax Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hypothalamus-pituitary axis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the head Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cornea Gene Set

From HPO Gene-Disease Associations

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

abnormality of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of metacarpophalangeal joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femoral neck or head region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the intrahepatic bile duct Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fluid regulation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the philtrum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dentate nucleus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pineal gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the crus of the helix Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the acetabulum Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sense of smell Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of central somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of permanent molar morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of muscle physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the parathyroid physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the achilles tendon Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thumb Gene Set

From HPO Gene-Disease Associations

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

abnormality of the myocardium Gene Set

From HPO Gene-Disease Associations

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

abnormality of complement system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the medullary cavity of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the renal tubule Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the shoulder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of chromosome condensation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prostaglandin metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neurodevelopmental abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of connective tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thumb phalanx Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the odontoid process Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of alanine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atlantoaxial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lower limb Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thrombocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the posterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thymus Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vestibulocochlear nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prenatal development or birth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper limb Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of binocular vision Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cation homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thyroid gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the bladder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the alveolar ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of forebrain morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the choroid plexus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of circulating protein level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pancreas morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the seventh cranial nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

biliary tract abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the lymphoid lineage Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the glial cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aryepiglottic fold Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cells of the erythroid lineage Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prothrombin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the subungual region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thyroid morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scalp Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the frontal hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the renal collecting system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pulmonary vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femoral metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of oral mucosa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nerves Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the acoustic reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of potassium homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pituitary gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubulointerstitial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dental pulp Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cysteine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thenar eminence Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of ganglioside metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of humoral immunity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sixth cranial nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of calvarial morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hip joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the humeral metaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of urine bicarbonate concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the genitourinary system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lymphatic vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fascia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the radius Gene Set

From HPO Gene-Disease Associations

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

abnormality of the liver Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of dental color Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of alkaline phosphatase activity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the larynx Gene Set

From HPO Gene-Disease Associations

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

chorioretinal abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating hormone level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the salivary glands Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of primary molar morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of copper homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sacroiliac joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the diaphragm Gene Set

From HPO Gene-Disease Associations

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

abnormality of movement Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lacrimal duct Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal tibial epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aortic valve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the corticospinal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the endocrine system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the endocrine system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the soft palate Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the adrenal glands Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the adrenal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the periorbital region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the periorbital region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the respiratory system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fontanelles Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the septum pellucidum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of renal excretion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of renal excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the premaxilla Gene Set

From HPO Gene-Disease Associations

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

eeg abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of renin-angiotensin system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of renin-angiotensin system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pancreas physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

c1-c2 vertebral abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lower lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pectoral muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pectoral muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of descemet's membrane Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of descemet's membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sclera Gene Set

From HPO Gene-Disease Associations

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

phenotypic abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating adrenocorticotropin level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating adrenocorticotropin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the radial head Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the radial head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of saccadic eye movements Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasolabial region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasolabial region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the uvea Gene Set

From HPO Gene-Disease Associations

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