Dysarthria

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Gene Set

Results for "Dysarthria": 15 gene sets

Name
Dysarthria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dysarthria from the curated CTD Gene-Disease Associations dataset.
dysarthria Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dysarthria in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
dysarthria Gene Set From HPO Gene-Disease Associations genes associated with the dysarthria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Dysarthria Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysarthria phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysarthria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysarthria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysarthria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysarthria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysarthria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dysarthria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations 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.
Pyramidal Dysarthria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Dysarthria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extrapyramidal Dysarthria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extrapyramidal Dysarthria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.