Name

Cerebral palsy, spastic quadriplegic, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.

cerebral palsy, spastic quadriplegic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral palsy, spastic quadriplegic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spastic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral hemorrhage; cerebral hemorrhages; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive 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.

Cerebral Palsy, Ataxic, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Ataxic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy Gene Set

From CTD Gene-Disease Associations

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

cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ataxic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dyskinetic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral palsy Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; hemiplegia Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; hemiplegia; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; hemiplegia; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy; pregnancy complications, infectious; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy Gene Set

From HPO Gene-Disease Associations

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

Cerebral Palsy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

quadriplegic Gene Set

From GeneRIF Biological Term Annotations

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

paraparesis, tropical spastic; tropical spastic paraparesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct; cerebral arteriopathy Gene Set

From GAD Gene-Disease Associations

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

apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Gaze palsy, familial horizontal, with progressive scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive, 2 from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive, 3 from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.

Bulbar Palsy, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bulbar Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.

Progressive supranuclear palsy atypical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Supranuclear Palsy, Progressive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

progressive supranuclear palsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease progressive supranuclear palsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bell's palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial third-nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive supranuclear palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fourth cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive bulbar palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pseudobulbar palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tibial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

conjugate gaze palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial atypical progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

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

neurodegenerative diseases; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

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

supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

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

dementia; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

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

chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vocal cord palsy Gene Set

From GAD Gene-Disease Associations

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

palsy Gene Set

From GeneRIF Biological Term Annotations

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

Progressive supranuclear palsy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

progressive supranuclear palsy Gene Set

From GWASdb SNP-Disease Associations

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

supranuclear gaze palsy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the supranuclear gaze palsy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vertical supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the vertical supranuclear gaze palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial palsy Gene Set

From HPO Gene-Disease Associations

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

paraganglioma-related cranial nerve palsy Gene Set

From HPO Gene-Disease Associations

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

abducens palsy Gene Set

From HPO Gene-Disease Associations

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

facial palsy secondary to cranial hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

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

horizontal supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the horizontal supranuclear gaze palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bulbar palsy Gene Set

From HPO Gene-Disease Associations

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

oculomotor nerve palsy Gene Set

From HPO Gene-Disease Associations

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

Bulbar Palsy, Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bulbar Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Supranuclear Palsy, Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Supranuclear Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

supranuclear palsy, progressive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive atypical Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

gaze palsy, horizontal, with progressive scoliosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaze palsy, horizontal, with progressive scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Spastic paraplegia 46, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 46, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 48, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 48, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 4, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 54, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 54, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 4, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 5A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 11, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 11, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 57, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 57, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 72, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 72, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 35 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 44, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 44, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia 5, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia 5, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 72, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 72, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia Charlevoix-Saguenay type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia Charlevoix-Saguenay type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 55, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 55, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 63, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 63, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 31, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 31, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 39 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 56, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 56, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 30, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 30, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 33, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 33, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 2, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 45, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 45, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile-onset ascending hereditary spastic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 42, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 42, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 24 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 24 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 20, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 20, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 32, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 32, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 36, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 36, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 34, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 34, X-Linked from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia type 5A, recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia type 5A, recessive from the curated CTD Gene-Disease Associations dataset.

Ataxia, Spastic, 3, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia, Spastic, 3, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 7, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 7, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Hereditary spastic paralysis, infantile onset ascending Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 4, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 4, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia type 5B, recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia type 5B, recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 31, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 31, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 16, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 16, X-linked from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 42, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 42, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 33, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 33, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 17 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 11, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 11, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 10, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 10, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 44, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 44, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 2, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 2, X-linked from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 25, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 25, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Paraparesis, Spastic Gene Set

From CTD Gene-Disease Associations

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

SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 15, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 15, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 39, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 39, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 9, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 9, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 37, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 37, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia-50, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia-50, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 3, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 3, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 38, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 38, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spastic ataxia Charlevoix-Saguenay type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic ataxia Charlevoix-Saguenay type from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 23 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 14, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 14, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 29, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 29, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 6, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 6, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 8, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 8, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Ataxia, Spastic, 1, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Hereditary from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 27, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 27, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 13, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 13, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 19, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 19, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 18, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 18, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

hereditary spastic paraplegia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

spastic quadriplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic hemiplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic entropion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic diplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary spastic paraplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic ectropion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tropical spastic paraparesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

motor neuron disease; paraparesis, spastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease motor neuron disease; paraparesis, spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spastic paraplegia Gene Set

From GAD Gene-Disease Associations

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

spastic paralysis Gene Set

From GAD Gene-Disease Associations

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

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-1 associated myelopathy/tropical spastic; paraparesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-1 associated myelopathy/tropical spastic; paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary spastic angina. Gene Set

From GAD Gene-Disease Associations

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

coronary spastic angina Gene Set

From GAD Gene-Disease Associations

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

myelopathy/tropical spastic paraparesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelopathy/tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spastic paraplegia, hereditary Gene Set

From GAD Gene-Disease Associations

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

infantile-onset ascending hereditary spastic paralysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; spastic paraplegia, hereditary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; paraparesis, tropical spastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spastic Gene Set

From GeneRIF Biological Term Annotations

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

spastic dysarthria Gene Set

From HPO Gene-Disease Associations

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

spastic ataxia Gene Set

From HPO Gene-Disease Associations

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

progressive spastic paraplegia Gene Set

From HPO Gene-Disease Associations

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

progressive spastic quadriplegia Gene Set

From HPO Gene-Disease Associations

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

spastic tetraplegia Gene Set

From HPO Gene-Disease Associations

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

spastic tetraparesis Gene Set

From HPO Gene-Disease Associations

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

spastic diplegia Gene Set

From HPO Gene-Disease Associations

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

spastic gait Gene Set

From HPO Gene-Disease Associations

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

spastic paraparesis Gene Set

From HPO Gene-Disease Associations

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

spastic paraplegia Gene Set

From HPO Gene-Disease Associations

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

Paraparesis, Tropical Spastic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Paraparesis, Tropical Spastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Paraparesis, Spastic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spastic Paraplegia, Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spastic Paraplegia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

spastic paraplegia 8, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 8, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 13, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 13, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 5a, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 5a, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 12, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 12, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 72, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 72, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 29, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 29, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 16, x-linked, complicated Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 16, x-linked, complicated phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 18, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory, with spastic paraplegia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 32, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 32, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 53, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 53, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 19, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 19, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 2, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 3, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 33, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 33, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 64 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 64 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 30, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 30, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 42, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 42, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 43, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 43, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 45, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 45, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 25, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 25, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 39, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 39, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 55, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 55, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 24, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 24, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 28, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 28, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 37, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 11, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 11, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 2, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 46, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 46, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 38, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 38, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 26, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 26, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 51, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 51, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 47, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 47, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 27, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 27, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 9, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 9, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 34, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 34, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 52, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 52, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 6, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 14, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 14, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 56, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 56, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia, optic atrophy, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 35, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 35, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 10, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 10, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 41, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 41, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 4, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 50, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 50, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 44, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 44, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 15, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 15, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 36, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 36, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 72, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 72, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 49, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 49, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 7, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 3a, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 3a, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 54, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 54, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

silver spastic paraplegia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the silver spastic paraplegia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, spastic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, spastic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, spastic, 5, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, spastic, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 61, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 61, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 48, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 48, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 57, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 57, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 31, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 31, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia, charlevoix-saguenay type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia, charlevoix-saguenay type phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paralysis, infantile onset ascending Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From Reactome Pathways

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

Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) pathway from the Reactome Pathways dataset.

Cerebral nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Cerebral cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Frontal pole, cerebral cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Frontal pole, cerebral cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

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

From ClinVar Gene-Phenotype Associations

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

Cerebral folate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypomyelination, global cerebral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination, global cerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Cerebral cavernous malformations 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral cavernous malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral cavernous malformations 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral cavernous malformations 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cerebral amyloid angiopathy, Icelandic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset.

Cerebral Infarction Gene Set

From CTD Gene-Disease Associations

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

Cerebral Amyloid Angiopathy, App-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, App-Related from the curated CTD Gene-Disease Associations dataset.

Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

Infarction, Middle Cerebral Artery Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Infarction, Middle Cerebral Artery from the curated CTD Gene-Disease Associations dataset.

Diffuse Cerebral Sclerosis of Schilder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diffuse Cerebral Sclerosis of Schilder from the curated CTD Gene-Disease Associations dataset.

Cerebral Cavernous Malformations 2 Gene Set

From CTD Gene-Disease Associations

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

Hypomyelination, Global Cerebral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomyelination, Global Cerebral from the curated CTD Gene-Disease Associations dataset.

Cerebral Amyloid Angiopathy Gene Set

From CTD Gene-Disease Associations

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

Cerebral Cavernous Malformations 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Cavernous Malformations 3 from the curated CTD Gene-Disease Associations dataset.

Cerebral Hemorrhage Gene Set

From CTD Gene-Disease Associations

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

Cerebral Amyloid Angiopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

cerebral degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cerebral arterial disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

cerebral angioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral primitive neuroectodermal tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral sarcoidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral atherosclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral malaria Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral convexity meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral creatine deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

transient cerebral ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anterior cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral neuroblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral arteritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral arterial disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral falx meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral ventricle cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral lipidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral amyloid angiopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral amyloid angiopathy-related hemorrhage. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy-related hemorrhage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; memory disorders; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral cavernous malformations Gene Set

From GAD Gene-Disease Associations

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

cerebral atherosclerosis Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct; stroke, lacunar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarct; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; thrombosis Gene Set

From GAD Gene-Disease Associations

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

hypertension; cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

microangiopathy- related cerebral damage (marcd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microangiopathy- related cerebral damage (marcd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, malaria related; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

cerebral arteriopathy Gene Set

From GAD Gene-Disease Associations

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

cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

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

cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

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

cerebral circulation Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral ischemia Gene Set

From GAD Gene-Disease Associations

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

cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

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

cerebral ischemic events Gene Set

From GAD Gene-Disease Associations

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

apoplexy; atherosclerosis; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; cerebral infarction; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; cerebral infarction; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; lipoprotein; cerebral infarct Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; lipoprotein; cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

cerebral small-vessel disease Gene Set

From GAD Gene-Disease Associations

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

toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral aging Gene Set

From GAD Gene-Disease Associations

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

antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; intracranial arteriovenous malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; intracranial arteriovenous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy; senile plaques Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; senile plaques in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cerebral arterial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter hyperintensities Gene Set

From GAD Gene-Disease Associations

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

malaria; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

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

malarial anemia and cerebral malaria Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; intracranial embolism and thrombosis Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary artery disease; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral amyloid angiopathy. Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherothrombotic cerebral infarction. Gene Set

From GAD Gene-Disease Associations

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

cerebral malaria Gene Set

From GAD Gene-Disease Associations

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

cerebral amyloid angiopathy; plaque, amyloid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral amyloid angiopathy; plaque, amyloid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarct, atherothrombotic Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cadasil; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cadasil; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; leukomalacia, periventricular; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; leukomalacia, periventricular; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral arteriopathy; leukoencephalopathy Gene Set

From GAD Gene-Disease Associations

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

brain edema; infarction, middle cerebral artery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter lesions Gene Set

From GAD Gene-Disease Associations

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

cerebral circulation in smokers Gene Set

From GAD Gene-Disease Associations

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

brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; recurrence; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; hypertension Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction, atherosclerotic Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; hypoxia-ischemia, brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction. Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; hypertension; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; cerebral arterial diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; cerebral arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, cerebral Gene Set

From GAD Gene-Disease Associations

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

infarction, middle cerebral artery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral Gene Set

From GeneRIF Biological Term Annotations

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

cerebral cortex tangential migration using cell-axon interactions Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex tangential migration using cell-axon interactions biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

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

cerebral cortex tangential migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex development Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex development biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex regionalization Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex regionalization biological process from the curated GO Biological Process Annotations dataset.

extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the extension of a leading process involved in cell motility in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex radially oriented cell migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex radially oriented cell migration biological process from the curated GO Biological Process Annotations dataset.

cell motility involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the cell motility involved in cerebral cortex radial glia guided migration 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.

cerebral cortex cell migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex cell migration biological process from the curated GO Biological Process Annotations dataset.

modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

layer formation in cerebral cortex Gene Set

From GO Biological Process Annotations

genes participating in the layer formation in cerebral cortex biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cell motility involved in cerebral cortex radial glia guided migration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell motility involved in cerebral cortex radial glia guided migration biological process from the curated GO Biological Process Annotations dataset.

substrate-dependent cerebral cortex tangential migration Gene Set

From GO Biological Process Annotations

genes participating in the substrate-dependent cerebral cortex tangential migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex gabaergic interneuron fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron fate commitment 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.

cerebral cortex gabaergic interneuron migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron migration biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex gabaergic interneuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex gabaergic interneuron differentiation biological process from the curated GO Biological Process Annotations dataset.

White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

cerebral arterial disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

hypointensity of cerebral white matter on mri Gene Set

From GWASdb SNP-Phenotype Associations

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

diffuse cerebral sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the diffuse cerebral sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

cerebral ischemia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral aneurysm Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral cortex Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in cerebral cortex relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

small cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

cerebral edema Gene Set

From HPO Gene-Disease Associations

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

cerebral aneurysm Gene Set

From HPO Gene-Disease Associations

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

cerebral white matter atrophy Gene Set

From HPO Gene-Disease Associations

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

cerebral venous thrombosis Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

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

cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

recurrent cerebral hemorrhage Gene Set

From HPO Gene-Disease Associations

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

diffuse demyelination of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse demyelination of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

cerebral amyloid angiopathy Gene Set

From HPO Gene-Disease Associations

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

diffuse swelling of cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse swelling of cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral calcification Gene Set

From HPO Gene-Disease Associations

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

cerebral ischemia Gene Set

From HPO Gene-Disease Associations

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

arteriosclerosis of small cerebral arteries Gene Set

From HPO Gene-Disease Associations

genes associated with the arteriosclerosis of small cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subcortical cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

tortuous cerebral arteries Gene Set

From HPO Gene-Disease Associations

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

cerebral vasculitis Gene Set

From HPO Gene-Disease Associations

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

increased cerebral lipofuscin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral vasculature Gene Set

From HPO Gene-Disease Associations

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

thick cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

cerebral hypomyelination Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral subcortex Gene Set

From HPO Gene-Disease Associations

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

cerebral degeneration Gene Set

From HPO Gene-Disease Associations

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

cerebral cortical neurodegeneration Gene Set

From HPO Gene-Disease Associations

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

diffuse cerebral sclerosis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral ventricles Gene Set

From HPO Gene-Disease Associations

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

cerebral hamartomata Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral hamartomata phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

cerebral hemorrhage Gene Set

From HPO Gene-Disease Associations

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

multifocal cerebral white matter abnormalities Gene Set

From HPO Gene-Disease Associations

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

cerebral cortical atrophy Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral cortex Gene Set

From HPO Gene-Disease Associations

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

cerebral dysmyelination Gene Set

From HPO Gene-Disease Associations

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

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

cerebral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

cerebral inclusion bodies Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

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

frontotemporal cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

hypointensity of cerebral white matter on mri Gene Set

From HPO Gene-Disease Associations

genes associated with the hypointensity of cerebral white matter on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cerebral Hemorrhage, Traumatic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Infarction Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Malaria, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Infarction, Middle Cerebral Artery Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infarction, Middle Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Toxoplasmosis, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Arterial Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Diffuse Cerebral Sclerosis of Schilder Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Diffuse Cerebral Sclerosis of Schilder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Dominance, Cerebral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Amyloid Angiopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Infarction, Anterior Cerebral Artery Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infarction, Anterior Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cerebral Ventricle Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cerebral Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

cerebral edema Gene Set

From MPO Gene-Phenotype Associations

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

ectopic cerebral cortex pyramidal cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic cerebral cortex pyramidal cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebral arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebral aqueduct morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent cerebral aqueduct Gene Set

From MPO Gene-Phenotype Associations

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

delaminated cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

decreased cerebral infarction size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

thickened cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

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

cerebral cortex pyramidal cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cerebral cortex pyramidal cell number Gene Set

From MPO Gene-Phenotype Associations

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

abnormal stratification in cerebral cortex Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal stratification in cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebral cortex morphology Gene Set

From MPO Gene-Phenotype Associations

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

cerebral aqueductal stenosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebral cortex pyramidal cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebral cortex pyramidal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cerebral infarction size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{malaria, cerebral, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

cerebral creatine deficiency syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperkeratotic cutaneous capillary-venous malformations associated with cerebral capillary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, dystonia, and cerebral hypomyelination Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral cavernous malformations-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral cavernous malformations-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy, dutch, italian, iowa, flemish, arctic variants phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral amyloid angiopathy, prnp-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral amyloid angiopathy, prnp-related phenotype from the curated OMIM Gene-Disease Associations dataset.

{malaria, cerebral, reduced risk of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {malaria, cerebral, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination, global cerebral Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination, global cerebral phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral-cerebellar-coloboma syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

{cerebral infarction, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

vasculopathy, retinal, with cerebral leukodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral-cortex Gene Set

From Phosphosite Textmining Biological Term Annotations

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

cerebral lobe Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral cortex Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

cerebral lobe Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral cortex Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral peduncle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral gyrus Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

right middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue right middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

embryonic cerebral cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral giant cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral gyrus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral granule cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral peduncle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral cortical neuron Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral gray matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral white matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

left middle cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue left middle cerebral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cerebral subcortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral artery Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

cerebral hemisphere Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

TG(20:3n6/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

TG(20:3n6/20:3n6/20:4(8Z,11Z,14Z,17Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:4(8Z,11Z,14Z,17Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:4(8Z,11Z,14Z,17Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:4(8Z,11Z,14Z,17Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:1(11Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:1(11Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(22:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(22:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:3(6Z,9Z,12Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:3(6Z,9Z,12Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(15:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(15:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/16:1(9Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/16:1(9Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:5(7Z,10Z,13Z,16Z,19Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:5(7Z,10Z,13Z,16Z,19Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:2n6/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:2n6/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(22:1(13Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(22:1(13Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/o-18:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/o-18:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/22:2(13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/22:2(13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(24:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(24:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/14:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/14:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/18:4(6Z,9Z,12Z,15Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/18:4(6Z,9Z,12Z,15Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:4(5Z,8Z,11Z,14Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:4(5Z,8Z,11Z,14Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(20:3n9/0:0/20:3n9) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(20:3n9/0:0/20:3n9) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:3n6/0:0/18:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:3n6/0:0/18:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3(5Z,8Z,11Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3(5Z,8Z,11Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:1(11Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:1(11Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(20:3n6/0:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(20:3n6/0:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/22:4(7Z,10Z,13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/22:4(7Z,10Z,13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:1(11Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:1(11Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:1(9Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:1(9Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/15:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/15:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(14:1(9Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(14:1(9Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(14:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(14:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/22:5(7Z,10Z,13Z,16Z,19Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/22:5(7Z,10Z,13Z,16Z,19Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/22:5(4Z,7Z,10Z,13Z,16Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/22:5(4Z,7Z,10Z,13Z,16Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:3n3/0:0/18:3n3) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:3n3/0:0/18:3n3) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:5(5Z,8Z,11Z,14Z,17Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:5(5Z,8Z,11Z,14Z,17Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:3(9Z,12Z,15Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:3(9Z,12Z,15Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:4(6Z,9Z,12Z,15Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:4(6Z,9Z,12Z,15Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:3(6Z,9Z,12Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:3(6Z,9Z,12Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:5(4Z,7Z,10Z,13Z,16Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:5(4Z,7Z,10Z,13Z,16Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/20:4(5Z,8Z,11Z,14Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:4(5Z,8Z,11Z,14Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/16:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/16:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/24:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/24:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

DG(18:3n6/0:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(18:3n6/0:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:1(11Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:1(11Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:2n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:2n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:2(9Z,12Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:2(9Z,12Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:1(13Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:1(13Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/o-18:0) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/o-18:0) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/14:1(9Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/14:1(9Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(24:1(15Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(24:1(15Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:1(9Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:1(9Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3(5Z,8Z,11Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3(5Z,8Z,11Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:4(7Z,10Z,13Z,16Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:4(7Z,10Z,13Z,16Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/24:1(15Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/24:1(15Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/18:2(9Z,12Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/18:2(9Z,12Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:2(13Z,16Z)/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:2(13Z,16Z)/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(16:1(9Z)/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(16:1(9Z)/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/18:3(9Z,12Z,15Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/18:3(9Z,12Z,15Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(16:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(16:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/22:0/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/22:0/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(20:3n6/20:3n6/20:5(5Z,8Z,11Z,14Z,17Z)) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:5(5Z,8Z,11Z,14Z,17Z)) metabolite from the curated HMDB Metabolites of Enzymes dataset.

TG(18:0/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(18:0/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes dataset.

layer III of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer III of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer VI of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer VI of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer IIIu of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer IIIu of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer IIIu of area 35r Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer IIIu of area 35r relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer V of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer V of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer II of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer II of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

nih 3T3 Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in nih 3T3 relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.

PPARG-20887899-3T3-L1 PREADIPOCYTE CELLS-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the PPARG-20887899-3T3-L1 PREADIPOCYTE CELLS-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

PPARG-19300518-3T3-L1 preadipocyte cells-mouse Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the PPARG-19300518-3T3-L1 preadipocyte cells-mouse transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Immunodeficiency 31C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 31C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency 31a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 31a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

carbenoxolone-3353 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the carbenoxolone-3353 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

securinine-3470 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the securinine-3470 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ribostamycin-3444 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ribostamycin-3444 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

equilin-3377 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the equilin-3377 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tonzonium bromide-3080 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tonzonium bromide-3080 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bambuterol-3199 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bambuterol-3199 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ganciclovir-3368 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ganciclovir-3368 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

famprofazone-3928 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the famprofazone-3928 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3868 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3868 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tyloxapol-3074 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tyloxapol-3074 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefoxitin-3477 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefoxitin-3477 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-320650-01-4382 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-320650-01-4382 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

amiloride-3990 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the amiloride-3990 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pilocarpine-3300 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pilocarpine-3300 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PNU-0230031-3632 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PNU-0230031-3632 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

diethylstilbestrol-3812 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the diethylstilbestrol-3812 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

acacetin-3767 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the acacetin-3767 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piperacillin-3763 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piperacillin-3763 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

novobiocin-342 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the novobiocin-342 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

finasteride-3641 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the finasteride-3641 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfadimethoxine-3441 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfadimethoxine-3441 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

beta-escin-3807 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the beta-escin-3807 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

betonicine-3642 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the betonicine-3642 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PNU-0251126-3692 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PNU-0251126-3692 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mepenzolate bromide-3748 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mepenzolate bromide-3748 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

promazine-3833 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the promazine-3833 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chloropyramine-3011 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chloropyramine-3011 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tropicamide-3619 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tropicamide-3619 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methazolamide-3474 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methazolamide-3474 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

helveticoside-3770 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the helveticoside-3770 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clotrimazole-3166 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clotrimazole-3166 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

flunisolide-3828 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the flunisolide-3828 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tolmetin-3347 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tolmetin-3347 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-1082-3530 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-1082-3530 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mexiletine-3862 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mexiletine-3862 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefsulodin-3328 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefsulodin-3328 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

apigenin-3257 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the apigenin-3257 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tretinoin-390 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tretinoin-390 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

flunixin-3713 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the flunixin-3713 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

meclofenoxate-3405 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the meclofenoxate-3405 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfanilamide-3449 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfanilamide-3449 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nizatidine-3047 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nizatidine-3047 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

liothyronine-3324 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the liothyronine-3324 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

theobromine-3334 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the theobromine-3334 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fluvastatin-3370 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fluvastatin-3370 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

doxazosin-3024 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the doxazosin-3024 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

amiprilose-3339 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the amiprilose-3339 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

simvastatin-3340 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the simvastatin-3340 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trimipramine-3004 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trimipramine-3004 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

exisulind-314 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the exisulind-314 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lithocholic acid-3899 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lithocholic acid-3899 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

citiolone-3836 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the citiolone-3836 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

terbutaline-3202 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the terbutaline-3202 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

proglumide-3972 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the proglumide-3972 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fludrocortisone-3866 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fludrocortisone-3866 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

saquinavir-3549 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the saquinavir-3549 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rofecoxib-371 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rofecoxib-371 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

eucatropine-3759 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the eucatropine-3759 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

naringin-3286 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the naringin-3286 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

aminohippuric acid-3076 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the aminohippuric acid-3076 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nizatidine-3385 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nizatidine-3385 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ioversol-3365 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ioversol-3365 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ambroxol-3238 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ambroxol-3238 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tinidazole-3896 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tinidazole-3896 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bergenin-3467 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bergenin-3467 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

flecainide-3418 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the flecainide-3418 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

staurosporine-312 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the staurosporine-312 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlorcyclizine-3893 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlorcyclizine-3893 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mephenesin-3675 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mephenesin-3675 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

guanadrel-3438 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the guanadrel-3438 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

flutamide-3885 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the flutamide-3885 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-35215-6380 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-35215-6380 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lansoprazole-3529 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lansoprazole-3529 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-319743-7537 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-319743-7537 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-319743-7532 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-319743-7532 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

karakoline-3638 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the karakoline-3638 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

glibenclamide-3163 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the glibenclamide-3163 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dobutamine-3206 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dobutamine-3206 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ketorolac-3110 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ketorolac-3110 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxybutynin-3168 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxybutynin-3168 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PHA-00851261E-3854 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PHA-00851261E-3854 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piperidolate-3551 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piperidolate-3551 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

azlocillin-3468 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the azlocillin-3468 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

indoprofen-3007 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the indoprofen-3007 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3791 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3791 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

2,6-dimethylpiperidine-3806 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2,6-dimethylpiperidine-3806 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfadoxine-3547 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfadoxine-3547 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3177 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3177 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

guanadrel-3698 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the guanadrel-3698 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

desipramine-3212 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the desipramine-3212 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

praziquantel-3189 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the praziquantel-3189 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

propofol-3386 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the propofol-3386 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

felbinac-3398 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the felbinac-3398 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tropine-3569 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tropine-3569 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dorzolamide-3565 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dorzolamide-3565 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

7-aminocephalosporanic acid-3258 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 7-aminocephalosporanic acid-3258 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dicoumarol-3941 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dicoumarol-3941 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

remoxipride-3124 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the remoxipride-3124 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

natamycin-3548 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the natamycin-3548 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

(+)-isoprenaline-3384 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the (+)-isoprenaline-3384 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

gossypol-3740 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the gossypol-3740 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

betulinic acid-3281 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the betulinic acid-3281 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sirolimus-362 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sirolimus-362 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dantrolene-3867 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dantrolene-3867 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

paracetamol-3364 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the paracetamol-3364 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piretanide-3567 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piretanide-3567 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ketotifen-3200 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ketotifen-3200 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

drofenine-3455 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the drofenine-3455 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

meclocycline-3277 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the meclocycline-3277 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

thioperamide-3392 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the thioperamide-3392 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

monorden-325 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the monorden-325 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

terguride-3082 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the terguride-3082 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ganciclovir-3030 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ganciclovir-3030 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clonidine-3172 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clonidine-3172 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

meclofenoxate-3605 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the meclofenoxate-3605 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

diclofenamide-3366 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the diclofenamide-3366 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mesalazine-3584 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mesalazine-3584 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tretinoin-3165 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tretinoin-3165 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

quinpirole-3539 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the quinpirole-3539 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

hydralazine-3724 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the hydralazine-3724 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

medrysone-3705 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the medrysone-3705 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

protriptyline-3119 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the protriptyline-3119 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

betonicine-3745 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the betonicine-3745 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3114 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3114 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

felodipine-3295 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the felodipine-3295 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

maprotiline-3236 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the maprotiline-3236 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

scopoletin-3131 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the scopoletin-3131 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

gramine-3999 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the gramine-3999 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

butacaine-3469 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the butacaine-3469 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlorogenic acid-3282 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlorogenic acid-3282 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nefopam-3730 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nefopam-3730 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

proglumide-3861 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the proglumide-3861 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ozagrel-3503 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ozagrel-3503 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dimethadione-3029 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dimethadione-3029 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

propranolol-3396 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the propranolol-3396 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-675-3682 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-675-3682 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fludrocortisone-3785 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fludrocortisone-3785 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

naftifine-3536 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the naftifine-3536 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

furaltadone-3413 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the furaltadone-3413 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ethaverine-3375 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ethaverine-3375 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bretylium tosilate-3394 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bretylium tosilate-3394 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichlormethiazide-3337 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichlormethiazide-3337 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

doxorubicin-3291 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the doxorubicin-3291 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

metamizole sodium-3835 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the metamizole sodium-3835 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

florfenicol-3083 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the florfenicol-3083 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

metoclopramide-3728 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the metoclopramide-3728 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tremorine-3196 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tremorine-3196 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

spiradoline-3901 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the spiradoline-3901 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

enilconazole-3139 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the enilconazole-3139 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

atropine methonitrate-3116 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the atropine methonitrate-3116 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxybuprocaine-3996 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxybuprocaine-3996 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

procarbazine-3533 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the procarbazine-3533 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-685-3683 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-685-3683 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

paracetamol-3025 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the paracetamol-3025 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfamethoxypyridazine-3711 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfamethoxypyridazine-3711 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-690334-01-3823 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-690334-01-3823 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-690334-01-3826 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-690334-01-3826 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pralidoxime-3066 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pralidoxime-3066 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

2-aminobenzenesulfonamide-3400 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2-aminobenzenesulfonamide-3400 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

progesterone-3287 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the progesterone-3287 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

levcycloserine-3870 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the levcycloserine-3870 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ethaverine-3037 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ethaverine-3037 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

debrisoquine-3207 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the debrisoquine-3207 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

penbutolol-3534 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the penbutolol-3534 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methapyrilene-3205 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methapyrilene-3205 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

famprofazone-3753 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the famprofazone-3753 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-319743-7491 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-319743-7491 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

eucatropine-3841 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the eucatropine-3841 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ribavirin-3142 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ribavirin-3142 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trapidil-3136 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trapidil-3136 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

doxycycline-3479 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the doxycycline-3479 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lorglumide-3079 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lorglumide-3079 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

esculin-3052 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the esculin-3052 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ethotoin-3809 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ethotoin-3809 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

luteolin-3041 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the luteolin-3041 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

citiolone-3930 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the citiolone-3930 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

solasodine-3924 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the solasodine-3924 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dexamethasone-374 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dexamethasone-374 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxybenzone-3092 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxybenzone-3092 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

serotonin-3311 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the serotonin-3311 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

beclometasone-3001 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the beclometasone-3001 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nipecotic acid-3121 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nipecotic acid-3121 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

crotamiton-3050 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the crotamiton-3050 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tribenoside-3507 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tribenoside-3507 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fusaric acid-3245 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fusaric acid-3245 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

3-acetylcoumarin-3382 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 3-acetylcoumarin-3382 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefixime-3247 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefixime-3247 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxaprozin-3794 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxaprozin-3794 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piperacillin-3420 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piperacillin-3420 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-665-3681 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-665-3681 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lumicolchicine-3254 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lumicolchicine-3254 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dicoumarol-3848 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dicoumarol-3848 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-35874-6561 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-35874-6561 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piperacillin-3845 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piperacillin-3845 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ursodeoxycholic acid-3105 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ursodeoxycholic acid-3105 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bretylium tosilate-3057 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bretylium tosilate-3057 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

iocetamic acid-3361 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the iocetamic acid-3361 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nifedipine-335 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nifedipine-335 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3979 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3979 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tinidazole-3813 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tinidazole-3813 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

phentolamine-3971 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the phentolamine-3971 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyclobenzaprine-3268 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclobenzaprine-3268 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfamethoxazole-3667 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfamethoxazole-3667 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pivmecillinam-3535 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pivmecillinam-3535 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

zaprinast-3226 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the zaprinast-3226 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alfaxalone-3135 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alfaxalone-3135 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

repaglinide-3558 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the repaglinide-3558 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxytetracycline-3170 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxytetracycline-3170 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ascorbic acid-3225 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ascorbic acid-3225 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lanatoside C-3771 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lanatoside C-3771 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

octopamine-3112 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the octopamine-3112 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tamoxifen-375 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tamoxifen-375 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pramocaine-3811 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pramocaine-3811 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-3077 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-3077 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

atractyloside-3695 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the atractyloside-3695 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

practolol-3204 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the practolol-3204 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

eucatropine-3416 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the eucatropine-3416 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dicloxacillin-3307 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dicloxacillin-3307 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-857-3016 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-857-3016 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

2,6-dimethylpiperidine-3889 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2,6-dimethylpiperidine-3889 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

guaifenesin-3814 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the guaifenesin-3814 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cloperastine-3408 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cloperastine-3408 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

iopromide-3481 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the iopromide-3481 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

imidurea-3522 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the imidurea-3522 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mepenzolate bromide-3829 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mepenzolate bromide-3829 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

primidone-3065 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the primidone-3065 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

vanoxerine-3240 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the vanoxerine-3240 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

levcycloserine-3789 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the levcycloserine-3789 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rolitetracycline-3369 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rolitetracycline-3369 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rilmenidine-3133 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rilmenidine-3133 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

carbenoxolone-3014 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the carbenoxolone-3014 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylergometrine-3222 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylergometrine-3222 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylbenzethonium chloride-3850 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylbenzethonium chloride-3850 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-320650-01-3825 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-320650-01-3825 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-320650-01-3822 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-320650-01-3822 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clofazimine-3239 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clofazimine-3239 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chloropyrazine-3570 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chloropyrazine-3570 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

helveticoside-3945 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the helveticoside-3945 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for S