Name

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.

complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

alveolar bone loss; periodontal attachment loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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

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

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.

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.

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.

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.

neuronal loss in the cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

neuronal loss in central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in central nervous system 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.

hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; fetal loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, high-frequency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, bilateral; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, bilateral; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

fetal loss, late; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome 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.

Neurological pain disorder_Dorsal Root Ganglia_GSE15041 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurological pain disorder_Dorsal Root Ganglia_GSE15041 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases 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.

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.

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.

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

From Biocarta Pathways

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

role of erk5 in neuronal survival pathway Gene Set

From Biocarta Pathways

proteins participating in the role of erk5 in neuronal survival pathway pathway from the Biocarta Pathways dataset.

Ceroid lipofuscinosis, neuronal, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis, neuronal, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 4B autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 4B autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile neuronal ceroid lipofuscinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis, neuronal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis, neuronal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis neuronal 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis neuronal 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

neuronal cell body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

neuronal cell body membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the neuronal cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

neuronal ribonucleoprotein granule Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

neuronal cell body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

neuronal ribonucleoprotein granule Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Ceroid lipofuscinosis, neuronal 1, infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.

Ceroid Lipofuscinosis, Neuronal, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 10 from the curated CTD Gene-Disease Associations dataset.

Ceroid lipofuscinosis, neuronal 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 8 from the curated CTD Gene-Disease Associations dataset.

Ceroid lipofuscinosis, neuronal 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 5 from the curated CTD Gene-Disease Associations dataset.

Ceroid Lipofuscinosis, Neuronal, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 2 from the curated CTD Gene-Disease Associations dataset.

Ceroid Lipofuscinosis, Neuronal, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 1 from the curated CTD Gene-Disease Associations dataset.

Ceroid Lipofuscinosis, Neuronal, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 6 from the curated CTD Gene-Disease Associations dataset.

Ceroid Lipofuscinosis, Neuronal, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid Lipofuscinosis, Neuronal, 7 from the curated CTD Gene-Disease Associations dataset.

Ceroid lipofuscinosis, neuronal 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 9 from the curated CTD Gene-Disease Associations dataset.

Neuronal Ceroid-Lipofuscinoses Gene Set

From CTD Gene-Disease Associations

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

neuronal ceroid lipofuscinosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease neuronal ceroid lipofuscinosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

neuronal ceroid lipofuscinosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neuronal ceroid-lipofuscinoses Gene Set

From GAD Gene-Disease Associations

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

intestinal neuronal dysplasia type b (ind b) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuronal hyperexcitability Gene Set

From GAD Gene-Disease Associations

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

variant late infantile neuronal ceroid lipofuscinosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuronal no synthase (nos1) gene polymorphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuronal no synthase (nos1) gene polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic neuronal cell death Gene Set

From GAD Gene-Disease Associations

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

neuronal Gene Set

From GeneRIF Biological Term Annotations

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

Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

regulation of short-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

neuronal action potential Gene Set

From GO Biological Process Annotations

genes participating in the neuronal action potential biological process from the curated GO Biological Process Annotations dataset.

gonadotrophin-releasing hormone neuronal migration to the hypothalamus Gene Set

From GO Biological Process Annotations

genes participating in the gonadotrophin-releasing hormone neuronal migration to the hypothalamus biological process from the curated GO Biological Process Annotations dataset.

regulation of neuronal action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neuronal action potential biological process from the curated GO Biological Process Annotations dataset.

neuronal ion channel clustering Gene Set

From GO Biological Process Annotations

genes participating in the neuronal ion channel clustering biological process from the curated GO Biological Process Annotations dataset.

neuronal signal transduction Gene Set

From GO Biological Process Annotations

genes participating in the neuronal signal transduction biological process from the curated GO Biological Process Annotations dataset.

neuronal-glial interaction involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the neuronal-glial interaction involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

commitment of neuronal cell to specific neuron type in forebrain Gene Set

From GO Biological Process Annotations

genes participating in the commitment of neuronal cell to specific neuron type in forebrain biological process from the curated GO Biological Process Annotations dataset.

regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

neuronal action potential propagation Gene Set

From GO Biological Process Annotations

genes participating in the neuronal action potential propagation biological process from the curated GO Biological Process Annotations dataset.

neuronal stem cell maintenance Gene Set

From GO Biological Process Annotations

genes participating in the neuronal stem cell maintenance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

regulation of neuronal signal transduction Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neuronal signal transduction biological process from the curated GO Biological Process Annotations dataset.

neuronal stem cell division Gene Set

From GO Biological Process Annotations

genes participating in the neuronal stem cell division biological process from the curated GO Biological Process Annotations dataset.

cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the cell-cell adhesion involved in neuronal-glial interactions involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

regulation of neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

neuronal cell body Gene Set

From GO Cellular Component Annotations

proteins localized to the neuronal cell body cellular component from the curated GO Cellular Component Annotations dataset.

neuronal cell body membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the neuronal cell body membrane cellular component from the curated GO Cellular Component Annotations dataset.

neuronal postsynaptic density Gene Set

From GO Cellular Component Annotations

proteins localized to the neuronal postsynaptic density cellular component from the curated GO Cellular Component Annotations dataset.

neuronal ribonucleoprotein granule Gene Set

From GO Cellular Component Annotations

proteins localized to the neuronal ribonucleoprotein granule cellular component from the curated GO Cellular Component Annotations dataset.

white matter neuronal heterotopia Gene Set

From HPO Gene-Disease Associations

genes associated with the white matter neuronal heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of neuronal migration Gene Set

From HPO Gene-Disease Associations

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

increased neuronal autofluorescent lipopigment Gene Set

From HPO Gene-Disease Associations

genes associated with the increased neuronal autofluorescent lipopigment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Neuronal Ceroid-Lipofuscinoses Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuronal migration protein doublecortin, chordata Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuronal migration protein doublecortin, chordata protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dopamine/cAMP-regulated neuronal phosphoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dopamine/cAMP-regulated neuronal phosphoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ceroid-lipofuscinosis neuronal protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ceroid-lipofuscinosis neuronal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ceroid-lipofuscinosis neuronal protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ceroid-lipofuscinosis neuronal protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuronal protein 3.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuronal protein 3.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cell cycle exit/neuronal differentiation protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cell cycle exit/neuronal differentiation protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1/2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

premature neuronal precursor differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature neuronal precursor differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

neuronal intranuclear inclusions Gene Set

From MPO Gene-Phenotype Associations

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

decreased neuronal stem cell self-renewal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to neuronal excitotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal stem cell self-renewal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal stem cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal neuronal layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased neuronal stem cell self-renewal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal stem cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to neuronal excitotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal migration Gene Set

From MPO Gene-Phenotype Associations

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

neuronal cytoplasmic inclusions Gene Set

From MPO Gene-Phenotype Associations

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

decreased neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

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

absent neuronal precursor cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent neuronal precursor cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal precursor proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neuronal precursor proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased neuronal precursor cell number Gene Set

From MPO Gene-Phenotype Associations

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

?ceroid lipofuscinosis, neuronal, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?ceroid lipofuscinosis, neuronal, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, kufs type, adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, kufs type, adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 4, parry type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 4, parry type phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 13, kufs type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 13, kufs type phenotype from the curated OMIM Gene-Disease Associations dataset.

intestinal pseudoobstruction, neuronal Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal pseudoobstruction, neuronal phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronal Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Lissencephaly gene (LIS1) in neuronal migration and development Gene Set

From PID Pathways

proteins participating in the Lissencephaly gene (LIS1) in neuronal migration and development pathway from the PID Pathways dataset.

Neuronal System Gene Set

From Reactome Pathways

proteins participating in the Neuronal System pathway from the Reactome Pathways dataset.

H3K4me3_H1 Derived Neuronal Progenitor Cultured Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_H1 Derived Neuronal Progenitor Cultured Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27ac_H1 Derived Neuronal Progenitor Cultured Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_H1 Derived Neuronal Progenitor Cultured Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

neuronal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

non-neuronal cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue non-neuronal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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

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

maintenance of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations

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

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

From GO Biological Process Annotations

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 dataset.

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

From GO Biological Process Annotations

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

establishment of epithelial cell apical/basal polarity Gene Set

From GO Biological Process Annotations

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

maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations

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

ciliary basal body organization Gene Set

From GO Biological Process Annotations

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

establishment of apical/basal cell polarity Gene Set

From GO Biological Process Annotations

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

establishment or maintenance of apical/basal cell polarity Gene Set

From GO Biological Process Annotations

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

basal cortex Gene Set

From GO Cellular Component Annotations

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

basal plasma membrane Gene Set

From GO Cellular Component Annotations

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

axonemal basal plate Gene Set

From GO Cellular Component Annotations

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

basal lamina Gene Set

From GO Cellular Component Annotations

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

basal part of cell Gene Set

From GO Cellular Component Annotations

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

ciliary basal body Gene Set

From GO Cellular Component Annotations

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

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

From GO Molecular Function Annotations

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

rna polymerase ii basal transcription factor binding Gene Set

From GO Molecular Function Annotations

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

basal rna polymerase ii transcription machinery binding Gene Set

From GO Molecular Function Annotations

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

basal transcription machinery binding Gene Set

From GO Molecular Function Annotations

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

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.

Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

DFNA 2 Nonsyndromic Hearing Loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the DFNA 2 Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hearing Loss, Sudden Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Sudden from the curated CTD Gene-Disease Associations dataset.

Blood Loss, Surgical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Loss, Surgical from the curated CTD Gene-Disease Associations dataset.

Hearing Loss Gene Set

From CTD Gene-Disease Associations

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

HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Tooth Loss Gene Set

From CTD Gene-Disease Associations

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

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.

Progressive hearing loss stapes fixation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Conductive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Conductive from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Sensorineural Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Sensorineural from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Weight Loss Gene Set

From CTD Gene-Disease Associations

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

Hearing Loss, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Bilateral from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Noise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Noise-Induced from the curated CTD Gene-Disease Associations dataset.

Alveolar Bone Loss Gene Set

From CTD Gene-Disease Associations

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

Embryo Loss Gene Set

From CTD Gene-Disease Associations

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

Hearing Loss Gene Set

From dbGAP Gene-Trait Associations

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

sensorineural hearing loss Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hearing loss Gene Set

From GAD Gene-Disease Associations

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

hypertension; overweight; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; overweight; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss/deafness; osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tooth loss Gene Set

From GAD Gene-Disease Associations

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

inflammation; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

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

gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; otosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; otosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; vestibular diseases Gene Set

From GAD Gene-Disease Associations

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

hip bone loss and fracture Gene Set

From GAD Gene-Disease Associations

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

aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, second trimester Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, second trimester in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, central Gene Set

From GAD Gene-Disease Associations

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

autosomal dominant hearing loss Gene Set

From GAD Gene-Disease Associations

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

bone neoplasms; hearing loss; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early postmenopausal bone loss at the spine. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mouth, edentulous; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

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

aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; fetal death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

obesity; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

h-ras allele loss Gene Set

From GAD Gene-Disease Associations

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

arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; coagulation disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; rhinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural nonsyndromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural nonsyndromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

goiter; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood loss, surgical Gene Set

From GAD Gene-Disease Associations

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

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, late Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; chronic periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dominant non-syndromic sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing disorders; hearing loss, high-frequency; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous dental implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

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

insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

goiter; hearing loss, sensorineural; vertigo Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural; vertigo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; weight loss Gene Set

From GAD Gene-Disease Associations

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

dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein loss Gene Set

From GAD Gene-Disease Associations

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

embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight loss Gene Set

From GAD Gene-Disease Associations

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

deafness; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, unilateral Gene Set

From GAD Gene-Disease Associations

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

body weight; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

unresolved loss or trauma Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

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

obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

polycystic ovary syndrome; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent 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.

periodontal attachment loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; embryo loss; hyperhomocysteinemia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; embryo loss; hyperhomocysteinemia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent; in vitro fertilization success Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, early Gene Set

From GAD Gene-Disease Associations

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

obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; infant, premature, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, inborn; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, inborn; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent early fetal loss Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss/deafness Gene Set

From GAD Gene-Disease Associations

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

nonsyndromic hearing loss Gene Set

From GAD Gene-Disease Associations

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

weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

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

fetal loss ; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, nonsyndromic sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, nonsyndromic sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent fetal loss Gene Set

From GAD Gene-Disease Associations

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

reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

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

fatty liver; insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatty liver; insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; embryo loss; infertility, female Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; embryo loss; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; habitual aborter nos; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; habitual aborter nos; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; hearing loss Gene Set

From GAD Gene-Disease Associations

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

body weight; fatty liver; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; fatty liver; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone loss Gene Set

From GAD Gene-Disease Associations

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

goiter; hearing loss, sensorineural; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low bone-mineral density and rapid postmenopausal bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; gram-negative bacterial infections; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gram-negative bacterial infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; weight loss; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; weight loss; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; dental fistula; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; dental fistula; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

lumen loss, late Gene Set

From GAD Gene-Disease Associations

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

aggressive periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, abdominal; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antisense paternal transcript and loss of imprinting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antisense paternal transcript and loss of imprinting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid; postoperative complications; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; postoperative complications; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

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

gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

unexplained foetal loss Gene Set

From GAD Gene-Disease Associations

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

eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss; noonan syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss; noonan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

presbycusis; hearing loss Gene Set

From GAD Gene-Disease Associations

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

recurrent pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

loss Gene Set

From GeneRIF Biological Term Annotations

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

regulation of water loss via skin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations dataset.

Weight loss (gastric bypass surgery) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

weight loss Gene Set

From GWASdb SNP-Phenotype Associations

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

loss of ability to walk Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of ability to walk in first decade Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in first decade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-frequency hearing loss Gene Set

From HPO Gene-Disease Associations

genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of eyelashes Gene Set

From HPO Gene-Disease Associations

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

loss of facial expression Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of voice Gene Set

From HPO Gene-Disease Associations

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

loss of subcutaneous adipose tissue in limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of subcutaneous adipose tissue in limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent loss of toenails and fingernails Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weight loss Gene Set

From HPO Gene-Disease Associations

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

loss of truncal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of truncal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

axonal loss Gene Set

From HPO Gene-Disease Associations

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

scalp hair loss Gene Set

From HPO Gene-Disease Associations

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

sudden central visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive central visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cranial nerve motor loss Gene Set

From HPO Gene-Disease Associations

genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of speech Gene Set

From HPO Gene-Disease Associations

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

nonprogressive visual loss Gene Set

From HPO Gene-Disease Associations

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

loss of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of primary teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord posterior columns myelin loss Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of ability to walk in early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

visual loss Gene Set

From HPO Gene-Disease Associations

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

loss of consciousness Gene Set

From HPO Gene-Disease Associations

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

loss of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral visual field loss Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of gluteal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of gluteal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal sensory loss of all modalities Gene Set

From HPO Gene-Disease Associations

genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive visual loss Gene Set

From HPO Gene-Disease Associations

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

loss of purkinje cells in the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adipose tissue loss Gene Set

From HPO Gene-Disease Associations

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

Blood Loss, Surgical Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Central Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Tooth Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Unilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Unilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Functional Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Weight Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Mixed Conductive-Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Mixed Conductive-Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Bilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Bilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Noise-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, High-Frequency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Periodontal Attachment Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Embryo Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Alveolar Bone Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

syndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

conductive hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

loss of gabaergic neurons Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to ototoxicity-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sensorineural hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of vibrissae Gene Set

From MPO Gene-Phenotype Associations

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

loss of glutamate neurons Gene Set

From MPO Gene-Phenotype Associations

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

loss of dopaminergic neurons Gene Set

From MPO Gene-Phenotype Associations

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

loss of hippocampal neurons Gene Set

From MPO Gene-Phenotype Associations

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

proximal convoluted tubule brush border loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

weight loss Gene Set

From MPO Gene-Phenotype Associations

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

decreased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

partial loss of secondary muscle spindle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nonsyndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to age-related hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature hair loss Gene Set

From MPO Gene-Phenotype Associations

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

loss of eyelid cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal dorsal hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal hair loss Gene Set

From MPO Gene-Phenotype Associations

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

progressive hair loss Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of cortex neurons Gene Set

From MPO Gene-Phenotype Associations

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

abnormal susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{pregnancy loss, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{bulimia nervosa, age of onset of weight loss in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.

{?hearing loss, cisplatin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, hearing loss, and neurodegeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

Loss of Function of SMAD4 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways dataset.

Loss of Function of TGFBR2 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways dataset.

Loss of Nlp from mitotic centrosomes Gene Set

From Reactome Pathways

proteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways dataset.

Loss of Function of TGFBR1 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways dataset.

Loss of proteins required for interphase microtubule organization from the centrosome Gene Set

From Reactome Pathways

proteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways dataset.

Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways dataset.

Loss of Function of SMAD2/3 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways dataset.