Filters:

Results for "Symptomatic Irreversible Pulpitis": 23 gene sets

Name

Symptomatic Irreversible Pulpitis Gene Set

From DisGeNET Gene-Disease Associations

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

Irreversible Pulpitis Gene Set

From DisGeNET Gene-Disease Associations

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

irreversible Gene Set

From GeneRIF Biological Term Annotations

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

pulpitis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

pulpitis Gene Set

From GeneRIF Biological Term Annotations

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

Pulpitis Gene Set

From DisGeNET Gene-Disease Associations

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

Reversible Pulpitis Gene Set

From DisGeNET Gene-Disease Associations

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

Pulpitis Gene Set

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

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

Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset.

symptomatic Gene Set

From GeneRIF Biological Term Annotations

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

symptomatic seizures Gene Set

From HPO Gene-Disease Associations

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

polyhydramnios, megalencephaly, and symptomatic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyhydramnios, megalencephaly, and symptomatic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symptomatic Carotid Artery Stenosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Symptomatic Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symptomatic Torsion Dystonia Gene Set

From DisGeNET Gene-Disease Associations

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

Symptomatic Generalized Epilepsy Gene Set

From DisGeNET Gene-Disease Associations

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

Symptomatic Epilepsy Gene Set

From DisGeNET Gene-Disease Associations

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

Aortic Stenosis Symptomatic Gene Set

From DisGeNET Gene-Disease Associations

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

Symptomatic Infantile Spasms Gene Set

From DisGeNET Gene-Disease Associations

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

Symptomatic Myoclonic Epilepsy Gene Set

From DisGeNET Gene-Disease Associations

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

Symptomatic Nystagmus Gene Set

From DisGeNET Gene-Disease Associations

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

Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT) Gene Set

From Reactome Pathways 2024

proteins participating in the Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT) pathway from the Reactome Pathways 2024 dataset.

polyhydramnios, megalencephaly, and symptomatic epilepsy Gene Set

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

genes co-occuring with the disease polyhydramnios, megalencephaly, and symptomatic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.