epileptic encephalopathy, early infantile, 8

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Results for "epileptic encephalopathy, early infantile, 8": 1001 gene sets

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epileptic encephalopathy, early infantile, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
Early infantile epileptic encephalopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early infantile epileptic encephalopathy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 28 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 26 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 27 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, early infantile, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic Encephalopathy, Early Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.
Epileptic Encephalopathy, Early Infantile, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 24 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 25 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 26 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 27 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 23 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, early infantile, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
?epileptic encephalopathy, early infantile, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy With Suppression Bursts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy With Suppression Bursts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Infantile Epileptic Encephalopathy, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Infantile Epileptic Encephalopathy, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early infantile epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early infantile epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early Infantile Epileptic Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early Infantile Epileptic Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epileptic dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epileptic dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
epileptic encephalopathy, early infanitle, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the epileptic encephalopathy, early infanitle, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Undetermined early-onset epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Undetermined early-onset epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early onset epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SNAP25-related early-onset developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SNAP25-related early-onset developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epileptic encephalopathy, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, Lennox-Gastaut type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epileptic encephalopathy, Lennox-Gastaut type from the curated CTD Gene-Disease Associations dataset.
epileptic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the epileptic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
epileptic encephalopathy, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
Epileptic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epileptic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epileptic Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Epileptic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 14 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 13 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 26 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Developmental and epileptic encephalopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 86 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 86 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 84 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 80 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 80 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 93 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 93 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 53 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 53 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 76 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 98 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 98 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 31A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 31A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 60 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 60 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 62 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 62 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 103 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 103 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 91 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 91 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 66 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 66 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 87 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 94 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 94 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 6B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 6B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 65 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 65 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 97 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 97 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 75 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 102 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 102 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 82 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 85 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 85 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 67 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 67 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 104 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 104 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 106 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 106 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 74 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 74 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 58 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 58 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 90 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 90 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 57 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 45 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 72 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 72 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 78 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 71 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 71 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 100 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 100 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 96 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 96 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 89 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 89 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 70 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental and epileptic encephalopathy 64 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental and epileptic encephalopathy 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocephaly and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocephaly and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the EEF1A2-related developmental and degenerative epileptic-dyskinetic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Genetic developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Unclassified developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Unclassified developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
BSCL2-related Developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the BSCL2-related Developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRIM8-related epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRIM8-related epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RYR3-related Epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RYR3-related Epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HCN2 related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HCN2 related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNA3-associated developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNA3-associated developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GABRA4-related developmental and epileptic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GABRA4-related developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
infantile encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Encephalopathy, Infantile Subacute, Of Leigh in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Syndromic Infantile Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic Infantile Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Galactosialidosis, early infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early myoclonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
early myoclonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Early Myoclonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Myoclonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early myoclonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early myoclonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
epileptic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term epileptic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
epileptic spasms Gene Set From HPO Gene-Disease Associations genes associated with the epileptic spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Epileptic Drop Attack Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epileptic Drop Attack in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epileptic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epileptic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prolonged Epileptic Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prolonged Epileptic Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Late-Onset Epileptic Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Late-Onset Epileptic Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epileptic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Epileptic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Non-Epileptic Convulsion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Non-Epileptic Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Metabolic epileptic disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Metabolic epileptic disorders pathway from the WikiPathways Pathways 2024 dataset.
Epileptic spasm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epileptic spasm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation with infantile enterocolitis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation with infantile enterocolitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Galactosialidosis, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Galactosialidosis, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine palmitoyltransferase II deficiency, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type II, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked infantile nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile myofibromatosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile myofibromatosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amish infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyloric stenosis, infantile hypertrophic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy 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.
Metachromatic leukodystrophy, late infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metachromatic leukodystrophy, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal neurodegeneration with facial dysmorphism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal neurodegeneration with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease, infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Liver failure acute infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Liver failure acute infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sting-associated vasculopathy, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sialic acid storage disease, severe infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune disease, multisystem, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinsonism-Dystonia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 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.
Ceroid lipofuscinosis, neuronal 1, infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.
Infantile polyarteritis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infantile polyarteritis from the curated CTD Gene-Disease Associations dataset.
LIVER FAILURE, INFANTILE, TRANSIENT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LIVER FAILURE, INFANTILE, TRANSIENT from the curated CTD Gene-Disease Associations dataset.
Refsum Disease, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.
Glaucoma 3, primary infantile, B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amish Infantile Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Hemangioma, capillary infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemangioma, capillary infantile from the curated CTD Gene-Disease Associations dataset.
Striatonigral degeneration infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 5 from the curated CTD Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spasms, Infantile from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic 1 from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.
Hypophosphatasia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Infantile from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
infantile onset spinocerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
infantile refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infantile refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal infantile encephalocardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal infantile encephalocardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neurofibromatosis 1; spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease neurofibromatosis 1; spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypophosphatasia Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypophosphatasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variant late infantile neuronal ceroid lipofuscinosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
infantile hypertrophic pyloric stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spasms, infantile Gene Set From GAD Gene-Disease Associations genes associated with the disease spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term infantile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
calcific stippling of infantile cartilaginous skeleton Gene Set From HPO Gene-Disease Associations genes associated with the calcific stippling of infantile cartilaginous skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile onset Gene Set From HPO Gene-Disease Associations genes associated with the infantile onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile hypercalcemia Gene Set From HPO Gene-Disease Associations genes associated with the infantile hypercalcemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile muscular hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile spasms Gene Set From HPO Gene-Disease Associations genes associated with the infantile spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
infantile axial hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the infantile axial hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spasms, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spasms, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infantile Apparent Life-Threatening Event Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infantile Apparent Life-Threatening Event phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Diarrhea, Infantile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Diarrhea, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
pyloric stenosis, infantile hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
amish infantile epilepsy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the amish infantile epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertriglyceridemia, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypertriglyceridemia, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
liver failure, transient infantile Gene Set From OMIM Gene-Disease Associations genes associated with the liver failure, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
?myofibromatosis, infantile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?myofibromatosis, infantile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercalcemia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypercalcemia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
nephronophthisis 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the nephronophthisis 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myofibromatosis, infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myofibromatosis, infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuroaxonal neurodegeneration, infantile, with facial dysmophism Gene Set From OMIM Gene-Disease Associations genes associated with the neuroaxonal neurodegeneration, infantile, with facial dysmophism phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinsonism-dystonia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
sting-associated vasculopathy, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?infantile liver failure syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?infantile liver failure syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{hemangioma, capillary infantile, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hemangioma, capillary infantile, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
nystagmus, infantile periodic alternating, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
hemangioma, capillary infantile, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the hemangioma, capillary infantile, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, infantile, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set From OMIM Gene-Disease Associations genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypophosphatasia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatasia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
juvenile polyposis syndrome, infantile form Gene Set From OMIM Gene-Disease Associations genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
sandhoff disease, infantile, juvenile, and adult forms Gene Set From OMIM Gene-Disease Associations genes associated with the sandhoff disease, infantile, juvenile, and adult forms phenotype from the curated OMIM Gene-Disease Associations dataset.
sialic acid storage disorder, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the sialic acid storage disorder, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
autoinflammation with infantile enterocolitis Gene Set From OMIM Gene-Disease Associations genes associated with the autoinflammation with infantile enterocolitis phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune disease, multisystem, infantile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set From OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.
striatonigral degeneration, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
glaucoma 3, primary infantile, b Gene Set From OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary infantile, b 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 CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.
Infantile Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Spasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Spasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Nystagmus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Nystagmus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Myofibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Myofibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Infantile Neuronal Ceroid Lipfuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Infantile Neuronal Ceroid Lipfuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hemangioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Severe Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Severe Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Scurvy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Scurvy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Disease, Multisystem, Infantile-Onset, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Disease, Multisystem, Infantile-Onset, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Infantile Neurological, Cutaneous, And Articular Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Hypophosphatasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Hypophosphatasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemangioma, Capillary Infantile Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemangioma, Capillary Infantile in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptogenic Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptogenic Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Infantile Spasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Infantile Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuronal Ceroid Lipofuscinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuronal Ceroid Lipofuscinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration, Infantile, Mitochondrial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration, Infantile, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Malignant Osteopetrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Malignant Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endemic Tyrolean Infantile Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Endemic Tyrolean Infantile Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amish Infantile Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amish Infantile Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Infantile Nystagmus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Refsum Disease (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Refsum Disease (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Infantile Myasthenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Onset Spinocerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Onset Spinocerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 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.
Infantile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystinosis, Infantile Nephropathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystinosis, Infantile Nephropathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fastkd2-Related Infantile Mitochondrial Encephalomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fastkd2-Related Infantile Mitochondrial Encephalomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Atopic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Globoid Cell Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Globoid Cell Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Sandhoff Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Sandhoff Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sting-Associated Vasculopathy, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sting-Associated Vasculopathy, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Digital Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Digital Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Liver Failure Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Liver Failure Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Constant Exotropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Constant Exotropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gm 2 Gangliosidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gm 2 Gangliosidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Infantile Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Infantile Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Monoplegic Infantile Cerebral Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Monoplegic Infantile Cerebral Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Gastroenteritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurologic, Endocrine, And Pancreatic Disease, Multisystem, Infantile-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Infantile Mitochondrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Infantile Mitochondrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Free Sialic Acid Storage Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Free Sialic Acid Storage Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmoplastic Infantile Astrocytoma And Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Infantile Astrocytoma And Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver Failure, Infantile, Transient Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver Failure, Infantile, Transient in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Muscular Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Muscular Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Diarrhea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Nystagmus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Nystagmus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Obesity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Axial Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Axial Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hemangioma, Capillary Infantile, Somatic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hemangioma, Capillary Infantile, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Colic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Colic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infantile Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infantile Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 pathway from the Reactome Pathways 2024 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 pathway from the Reactome Pathways 2024 dataset.
COX deficiency, infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile Refsum disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile Refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile parkinsonism-dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile parkinsonism-dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypophosphatasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Seborrheic infantile dermatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile myofibromatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile myofibromatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient infantile liver failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient infantile liver failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial infantile seizures 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial infantile seizures 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypotonia with psychomotor retardation and characteristic facies-3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypotonia with psychomotor retardation and characteristic facies-3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile histiocytoid cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile histiocytoid cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile liver failure syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile liver failure syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile GM1 gangliosidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-infantile neuronal ceroid lipofuscinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-infantile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic infantile neurological Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic infantile neurological phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset ascending hereditary spastic paralysis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile onset spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile onset spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal/infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal/infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephronophthisis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Capillary infantile hemangioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary infantile hemangioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign sporadic infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign sporadic infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LAMB2-related infantile-onset nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LAMB2-related infantile-onset nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cortical hyperostosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile nephropathic cystinosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile nephropathic cystinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile spasms Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile spasms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile convulsions and choreoathetosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile convulsions and choreoathetosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile myofibromatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile myofibromatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile Nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile Nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Self-limited familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal Infantile Cardioencephalomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal Infantile Cardioencephalomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Periodic fever-infantile enterocolitis-autoinflammatory syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever-infantile enterocolitis-autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile osteopetrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile osteopetrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IL21-related infantile inflammatory bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IL21-related infantile inflammatory bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile or childhood onset neurodegenerative disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile liver failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile liver failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset generalized dyskinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset generalized dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive infantile hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive infantile hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient infantile hypertriglyceridemia and hepatosteatosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient infantile hypertriglyceridemia and hepatosteatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Episodic kinesigenic dyskinesia and familial infantile convulsions Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic kinesigenic dyskinesia and familial infantile convulsions phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial infantile bilateral striatal necrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial infantile bilateral striatal necrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ethylmalonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ethylmalonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertensive Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertensive Encephalopathy from the curated CTD Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Encephalopathy from the curated CTD Gene-Disease Associations dataset.
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Wernicke Encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wernicke Encephalopathy from the curated CTD Gene-Disease Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Mitochondrial neurogastrointestinal encephalopathy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial neurogastrointestinal encephalopathy syndrome from the curated CTD Gene-Disease Associations dataset.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
Spongiform Encephalopathy with Neuropsychiatric Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spongiform Encephalopathy with Neuropsychiatric Features from the curated CTD Gene-Disease Associations dataset.
Ethylmalonic encephalopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ethylmalonic encephalopathy from the curated CTD Gene-Disease Associations dataset.
glycine encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycine encephalopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycine encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycine encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hepatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
wernicke encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease wernicke encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
toxic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease toxic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypertensive encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypertensive encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic toxic encephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic toxic encephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatic encephalopathy; liver cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatic encephalopathy; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
encephalopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term encephalopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
hypoglycemic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the hypoglycemic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hepatic encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the hepatic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acute encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the acute encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mitochondrial encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the mitochondrial encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acute necrotizing encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the acute necrotizing encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Encephalopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Encephalopathy, Bovine Spongiform Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Encephalopathy, Bovine Spongiform phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
spongiform encephalopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spongiform encephalopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set From OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
ethylmalonic encephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the ethylmalonic encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, neonatal severe Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
glycine encephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the glycine encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective ACY1 causes encephalopathy Gene Set From Reactome Pathways 2014 proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways dataset.
Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ethylmalonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ethylmalonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spongiform Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spongiform Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoxic-Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoxic-Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Encephalopathy With Parasomnia And Obstructive Sleep Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biotin-Responsive Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biotin-Responsive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
3-Methylglutaconic Aciduria Type Iv With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 3-Methylglutaconic Aciduria Type Iv With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uremic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uremic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arsenic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arsenic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minimal Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minimal Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Reversible Encephalopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Reversible Encephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Traumatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Traumatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wernicke Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wernicke Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Static Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Static Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Necrotizing Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Necrotizing Encephalopathy Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transmissible Mink Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transmissible Mink Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Encephalopathy With Neuroserpin Inclusion Bodies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Encephalopathy With Neuroserpin Inclusion Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mercury Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mercury Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Hepatic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Febrile Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Febrile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Profound Static Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Static Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Neurogastrointestinal Encephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spongiform Encephalopathy With Neuropsychiatric Features Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spongiform Encephalopathy With Neuropsychiatric Features in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acute Necrotizing Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Necrotizing Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scn8A-Related Epilepsy With Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scn8A-Related Epilepsy With Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infanctile Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infanctile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycine Encephalopathy With Normal Serum Glycine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycine Encephalopathy With Normal Serum Glycine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infanctile Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infanctile Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
spongiform encephalopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spongiform encephalopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
encephalopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the encephalopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Ethylmalonic encephalopathy Gene Set From WikiPathways Pathways 2024 proteins participating in the Ethylmalonic encephalopathy pathway from the WikiPathways Pathways 2024 dataset.
Defective ACY1 causes encephalopathy Gene Set From Reactome Pathways 2024 proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways 2024 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Glycine encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Glycine encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial encephalopathy with neuroserpin inclusion bodies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ethylmalonic encephalopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ethylmalonic encephalopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Toxic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Toxic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic traumatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic traumatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ethylmalonic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ethylmalonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hepatic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertensive encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertensive encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Wernicke encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Wernicke encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycine encephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycine encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
TANGO2-related metabolic encephalopathy and arrythmias Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease TANGO2-related metabolic encephalopathy and arrythmias in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial encephalopathy with neuroserpin inclusion bodies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Encephalopathy due to defective mitochondrial and peroxisomal fission 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ethylmalonic encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ethylmalonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial acute necrotizing encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial acute necrotizing encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycine encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycine encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spongiform encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongiform encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to GLUT1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to GLUT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal Encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to defective mitochondrial and peroxisomal fission phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atypical glycine encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical glycine encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalitis/encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalitis/encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SYNGAP1-related encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SYNGAP1-related encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy, reducing body, X-linked, early-onset, severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 20, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sarcoidosis, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sarcoidosis, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 6, autosomal recessive early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular degeneration, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast cancer, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast cancer, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary myopathy with early respiratory failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
early endosome lumen Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the early endosome lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
early phagosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the early phagosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
early endosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the early endosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
early endosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
early phagosome membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the early phagosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
early phagosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the early phagosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
early endosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the early endosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
early endosome membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the early endosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
early recombination nodule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the early recombination nodule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.
Hereditary Myopathy with Early Respiratory Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.
Sarcoidosis, Early-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoidosis, Early-Onset from the curated CTD Gene-Disease Associations dataset.
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.
Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.
Parkinsonism, early onset with mental retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.
early yaws Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early yaws in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early invasive cervical adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early invasive cervical adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
early coronary disease. Gene Set From GAD Gene-Disease Associations genes associated with the disease early coronary disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
humoral responses to early food allergens in children Gene Set From GAD Gene-Disease Associations genes associated with the disease humoral responses to early food allergens in children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early postmenopausal bone loss at the spine. Gene Set From GAD Gene-Disease Associations genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset alcoholism/substance abuse. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset alcoholism/substance abuse. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrence and early onset of venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammatory bowel disease (early onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammatory bowel disease (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early polyarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease early polyarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset familial alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontitis, early-onset Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontitis, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temperament in early childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease temperament in early childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early cognitive decline Gene Set From GAD Gene-Disease Associations genes associated with the disease early cognitive decline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early marginal bone loss around endosseous dental implants. Gene Set From GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset prostate cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
altered lipid oxidation and early insulin secretion Gene Set From GAD Gene-Disease Associations genes associated with the disease altered lipid oxidation and early insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of esrf in pkd1 adult polycystic kidney disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of esrf in pkd1 adult polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction (early onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glaucoma, early-onset Gene Set From GAD Gene-Disease Associations genes associated with the disease glaucoma, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, early Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial early onset psoriasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity (early onset extreme) Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity (early onset extreme) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of sudden infant death. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conversion from colorectal adenoma to early carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease conversion from colorectal adenoma to early carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset ischemic heart disease. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset ischemic heart disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent early fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-stage breast cancers Gene Set From GAD Gene-Disease Associations genes associated with the disease early-stage breast cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced early insulin response to oral glucose Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset aggressive diffuse amyloidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset aggressive diffuse amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early marginal bone loss around endosseous implants. Gene Set From GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, early onset primary Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of multiple sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early occlusion of coronary by-pass Gene Set From GAD Gene-Disease Associations genes associated with the disease early occlusion of coronary by-pass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature ovarian failure; menopause, early Gene Set From GAD Gene-Disease Associations genes associated with the disease premature ovarian failure; menopause, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertension of early onset. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease early osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term early in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
negative regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2015 dataset.
early endosome to golgi transport Gene Set From GO Biological Process Annotations 2015 genes participating in the early endosome to golgi transport biological process from the curated GO Biological Process Annotations 2015 dataset.
protein localization to early endosome Gene Set From GO Biological Process Annotations 2015 genes participating in the protein localization to early endosome biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset.
early endosome lumen Gene Set From GO Cellular Component Annotations 2015 proteins localized to the early endosome lumen cellular component from the curated GO Cellular Component Annotations 2015 dataset.
cytoplasmic side of early endosome membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cytoplasmic side of early endosome membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
early phagosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the early phagosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
early endosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the early endosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
early endosome membrane Gene Set From GO Cellular Component Annotations 2015 proteins localized to the early endosome membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset.
Prostate cancer (early onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Prostate cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Monocyte early outgrowth colony forming units Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Monocyte early outgrowth colony forming units phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Obesity (early onset extreme) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Obesity (early onset extreme) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Inflammatory bowel disease (early onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Inflammatory bowel disease (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Myocardial infarction (early onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Myocardial infarction (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Breast cancer (early onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Breast cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
recurrent infections in infancy and early childhood Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
early balding Gene Set From HPO Gene-Disease Associations genes associated with the early balding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of ability to walk in early childhood Gene Set From HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
early onset of sexual maturation Gene Set From HPO Gene-Disease Associations genes associated with the early onset of sexual maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in early adulthood Gene Set From HPO Gene-Disease Associations genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Retrieval of early ER protein Rer1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retrieval of early ER protein Rer1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Radiation-inducible immediate-early gene IEX-1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Radiation-inducible immediate-early gene IEX-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Immediate early response Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Immediate early response protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protein LIN-9/Protein ALWAYS EARLY Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset.
early endosome Gene Set From LOCATE Curated Protein Localization Annotations proteins localized to the early endosome cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.
early vaginal opening Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early vaginal opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
early reproductive senescence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early reproductive senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
early parturition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
early sexual maturation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early sexual maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
early eyelid opening Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early eyelid opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
early cellular replicative senescence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the early cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
macular degeneration, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, early-onset, with fatal cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set From OMIM Gene-Disease Associations genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, mild, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
breast cancer, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the breast cancer, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
hepatic failure, early onset, and neurologic disorder Gene Set From OMIM Gene-Disease Associations genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
inflammatory bowel disease 25, early onset, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the inflammatory bowel disease 25, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set From OMIM Gene-Disease Associations genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.
{obesity, early-onset, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {obesity, early-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, proximal, with early respiratory muscle involvement Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
chondrocalcinosis with early-onset osteoarthritis Gene Set From OMIM Gene-Disease Associations genes associated with the chondrocalcinosis with early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.
inflammatory bowel disease 28, early onset, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the inflammatory bowel disease 28, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
sarcoidosis, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the sarcoidosis, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{major affective disorder 3, early onset} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset.
growth retardation, developmental delay, coarse facies, and early death Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.
osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set From OMIM Gene-Disease Associations genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinson disease 6, early onset Gene Set From OMIM Gene-Disease Associations genes associated with the parkinson disease 6, early onset phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinson disease 7, autosomal recessive early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the parkinson disease 7, autosomal recessive early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinson disease 20, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the parkinson disease 20, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary disease, chronic obstructive, severe early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, severe early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, early-onset atypical, with myoclonic features Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.
immediate-early-proteins Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term immediate-early-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Formation of the Early Elongation Complex Gene Set From Reactome Pathways 2014 proteins participating in the Formation of the Early Elongation Complex pathway from the Reactome Pathways dataset.
Phagosomal maturation (early endosomal stage) Gene Set From Reactome Pathways 2014 proteins participating in the Phagosomal maturation (early endosomal stage) pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the early endosome membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways dataset.
Regulation of APC/C activators between G1/S and early anaphase Gene Set From Reactome Pathways 2014 proteins participating in the Regulation of APC/C activators between G1/S and early anaphase pathway from the Reactome Pathways dataset.
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set From Reactome Pathways 2014 proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset.
Regulation of gene expression in early pancreatic precursor cells Gene Set From Reactome Pathways 2014 proteins participating in the Regulation of gene expression in early pancreatic precursor cells pathway from the Reactome Pathways dataset.
Early Phase of HIV Life Cycle Gene Set From Reactome Pathways 2014 proteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways dataset.
G0 and Early G1 Gene Set From Reactome Pathways 2014 proteins participating in the G0 and Early G1 pathway from the Reactome Pathways dataset.
Formation of the HIV-1 Early Elongation Complex Gene Set From Reactome Pathways 2014 proteins participating in the Formation of the HIV-1 Early Elongation Complex pathway from the Reactome Pathways dataset.
Early Rheumatoid Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Rheumatoid Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early-Stage Breast Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early-Stage Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Gastric Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Gastric Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scid Due To Ada Deficiency, Early-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scid Due To Ada Deficiency, Early-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Caries Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Syphilis, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Syphilis, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early-Onset Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early-Onset Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Schizophrenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Schizophrenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Radiation Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Radiation Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Repolarization Associated With Ventricular Fibrillation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Repolarization Associated With Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Early-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Early-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early T Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early T Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Inflammatory Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Inflammatory Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Disseminated Lyme Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Disseminated Lyme Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Copd, Severe Early-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Copd, Severe Early-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Myopathy With Early Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Myopathy With Early Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Psoriasis Type 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Psoriasis Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prefibrotic/Early Primary Myelofibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prefibrotic/Early Primary Myelofibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klhl9-Related Early-Onset Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Epilepsy, Myoclonic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early-Onset Lafora Body Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early-Onset Lafora Body Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Pregnancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Pregnancy Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Pregnancy Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death In Early Adulthood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Early Adulthood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Awakening Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Awakening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Balding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Balding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Severe Fetal Akinesia Sequence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Severe Fetal Akinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Infections In Infancy And Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Ability To Walk In Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Chronotype Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Chronotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Ossification Of Capital Femoral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Ossification Of Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Fontanel Closure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Fontanel Closure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Menarche Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Menarche in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Onset Of Sexual Maturation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Onset Of Sexual Maturation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Satiety Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Satiety in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Complication Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Complication in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early-Onset Coronary Artery Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Coronary Artery Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
early endosome to Golgi transport Gene Set From GO Biological Process Annotations 2023 genes participating in the early endosome to Golgi transport biological process from the curated GO Biological Process Annotations 2023 dataset.
early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
protein localization to early endosome Gene Set From GO Biological Process Annotations 2023 genes participating in the protein localization to early endosome biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2023 dataset.
otolith mineralization completed early in development Gene Set From GO Biological Process Annotations 2023 genes participating in the otolith mineralization completed early in development biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2023 dataset.
early endosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the early endosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
early endosome membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the early endosome membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
early phagosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the early phagosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
cytoplasmic side of early endosome membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the cytoplasmic side of early endosome membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
early endosome lumen Gene Set From GO Cellular Component Annotations 2023 proteins localized to the early endosome lumen cellular component from the curated GO Cellular Component Annotations 2023 dataset.
early phagosome membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the early phagosome membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
postsynaptic early endosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the postsynaptic early endosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
extrinsic component of postsynaptic early endosome membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the extrinsic component of postsynaptic early endosome membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
postsynaptic early endosome membrane Gene Set From GO Cellular Component Annotations 2023 proteins localized to the postsynaptic early endosome membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset.
early eyelid opening Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early eyelid opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early sexual maturation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early sexual maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early reproductive senescence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early reproductive senescence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early cellular replicative senescence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early cellular replicative senescence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early exit from anagen phase Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early exit from anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early parturition Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early parturition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early vaginal opening Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early vaginal opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased early germinal center B cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased early germinal center B cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased early germinal center B cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased early germinal center B cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
early balanopreputial separation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the early balanopreputial separation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased early germinal center B cell number Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased early germinal center B cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
increased early germinal center B cell number Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased early germinal center B cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Human - Bone Marrow - L2 - Early Erythroid Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Bone Marrow - L2 - Early Erythroid cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - Early GC-commited MYC+ Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Early GC-commited MYC+ cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - Early PC precursor Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Early PC precursor cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - IgM+ early PC precursor Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - IgM+ early PC precursor cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - LZ-DZ-re-entry early commitment Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - LZ-DZ-re-entry early commitment cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - PB committed early PC precursor Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - PB committed early PC precursor cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - Early MBC Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Early MBC cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Tonsil - L2 - MBC derived early PC precursor Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - MBC derived early PC precursor cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
postsynaptic early endosome Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term postsynaptic early endosome from the SynGO Synaptic Gene Annotations dataset.
extrinsic component of postsynaptic early endosome membrane Gene Set From SynGO Synaptic Gene Annotations genes associated with the synaptic term extrinsic component of postsynaptic early endosome membrane from the SynGO Synaptic Gene Annotations dataset.
Early hematopoietic cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early hematopoietic cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early effector T cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early effector T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early activated CD8+ T cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early activated CD8+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early activated CD4+ T cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early activated CD4+ T cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early mesenchymal cell_Bone_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early mesenchymal cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early digit Condensations_Bone_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early digit Condensations_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early osteoblastic cell_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early osteoblastic cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early erythroid cell_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early erythroid cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early mesenchymal progenitor cell_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early mesenchymal progenitor cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early neutrophil_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early neutrophil_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early megakaryocyte progenitor cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early megakaryocyte progenitor cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early erythroid progenitor cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early erythroid progenitor cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early myeloid cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early myeloid cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early B cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early B cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early CD34+ megakaryocyte-erythroid progenitor cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early CD34+ megakaryocyte-erythroid progenitor cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early-erythroblast_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early-erythroblast_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early neuroblast_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early neuroblast_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early intermediate precursor cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early intermediate precursor cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early GABAergic neuron_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early GABAergic neuron_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early differentiative tumor cell_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early differentiative tumor cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early oligodendrocyte_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early oligodendrocyte_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early cardiovascular progenitor cell_Embryonic heart_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early cardiovascular progenitor cell_Embryonic heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early mesenchymal cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early mesenchymal cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early progenitor cell_Lateral ganglionic eminence_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early progenitor cell_Lateral ganglionic eminence_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early vascular cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early vascular cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early endothelial cell_Heart_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early endothelial cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early enterocyte precursor cell_Intestinal crypt_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early enterocyte precursor cell_Intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early proximal tubule cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early proximal tubule cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early hemangioblast_Embryonic Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early hemangioblast_Embryonic Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early erythrocyte_Fetal liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early erythrocyte_Fetal liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early erythrocyte_Fetal liver_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early erythrocyte_Fetal liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early type I alveolar pneumocyte_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early type I alveolar pneumocyte_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early cranial neural crest cell_Soft palate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early cranial neural crest cell_Soft palate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early perimysial cell_Soft palate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early perimysial cell_Soft palate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early germ cell_Fetal ovary_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early germ cell_Fetal ovary_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early plasma cell_Pancreas_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early plasma cell_Pancreas_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early transit-amplifying prostate epithelial cell_Prostate_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early transit-amplifying prostate epithelial cell_Prostate_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early T cell progenitor (ETP)_Thymus_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early T cell progenitor (ETP)_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early secretory cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early secretory cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early myoblast_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early myoblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Early response secretory cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early response secretory cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Set From Reactome Pathways 2024 proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways 2024 dataset.
Activation of anterior HOX genes in hindbrain development during early embryogenesis Gene Set From Reactome Pathways 2024 proteins participating in the Activation of anterior HOX genes in hindbrain development during early embryogenesis pathway from the Reactome Pathways 2024 dataset.
Early Phase of HIV Life Cycle Gene Set From Reactome Pathways 2024 proteins participating in the Early Phase of HIV Life Cycle pathway from the Reactome Pathways 2024 dataset.
Early SARS-CoV-2 Infection Events Gene Set From Reactome Pathways 2024 proteins participating in the Early SARS-CoV-2 Infection Events pathway from the Reactome Pathways 2024 dataset.
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis Gene Set From Reactome Pathways 2024 proteins participating in the FBXL7 down-regulates AURKA during mitotic entry and in early mitosis pathway from the Reactome Pathways 2024 dataset.
Formation of the Early Elongation Complex Gene Set From Reactome Pathways 2024 proteins participating in the Formation of the Early Elongation Complex pathway from the Reactome Pathways 2024 dataset.
Formation of the HIV-1 Early Elongation Complex Gene Set From Reactome Pathways 2024 proteins participating in the Formation of the HIV-1 Early Elongation Complex pathway from the Reactome Pathways 2024 dataset.
G0 and Early G1 Gene Set From Reactome Pathways 2024 proteins participating in the G0 and Early G1 pathway from the Reactome Pathways 2024 dataset.
HCMV Early Events Gene Set From Reactome Pathways 2024 proteins participating in the HCMV Early Events pathway from the Reactome Pathways 2024 dataset.
Regulation of APC/C activators between G1/S and early anaphase Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of APC/C activators between G1/S and early anaphase pathway from the Reactome Pathways 2024 dataset.
Regulation of gene expression in early pancreatic precursor cells Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of gene expression in early pancreatic precursor cells pathway from the Reactome Pathways 2024 dataset.
Synthesis of PIPs at the early endosome membrane Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways 2024 dataset.
early endosome to Golgi transport Gene Set From GO Biological Process Annotations 2025 genes participating in the early endosome to Golgi transport biological process from the curated GO Biological Process Annotations 2025 dataset.
early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
protein localization to early endosome Gene Set From GO Biological Process Annotations 2025 genes participating in the protein localization to early endosome biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2025 dataset.
early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of early endosome to late endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of early endosome to late endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of early endosome to recycling endosome transport Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of early endosome to recycling endosome transport biological process from the curated GO Biological Process Annotations 2025 dataset.
otolith mineralization completed early in development Gene Set From GO Biological Process Annotations 2025 genes participating in the otolith mineralization completed early in development biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of protein localization to early endosome Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of protein localization to early endosome biological process from the curated GO Biological Process Annotations 2025 dataset.
early endosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the early endosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
early endosome membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the early endosome membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
early phagosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the early phagosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
cytoplasmic side of early endosome membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the cytoplasmic side of early endosome membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
early endosome lumen Gene Set From GO Cellular Component Annotations 2025 proteins localized to the early endosome lumen cellular component from the curated GO Cellular Component Annotations 2025 dataset.
early phagosome membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the early phagosome membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
extrinsic component of postsynaptic early endosome membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the extrinsic component of postsynaptic early endosome membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
postsynaptic early endosome membrane Gene Set From GO Cellular Component Annotations 2025 proteins localized to the postsynaptic early endosome membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset.
early-onset Parkinson's disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset Parkinson's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber congenital amaurosis with early-onset deafness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber congenital amaurosis with early-onset deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early yaws Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early yaws in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset vitamin B6-dependent epilepsy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset vitamin B6-dependent epilepsy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early congenital syphilis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early invasive cervical adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early invasive cervical adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early endosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Early endosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Early endosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Early phagosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Early phagosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Cytoplasmic side of early endosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cytoplasmic side of early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Early phagosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Early phagosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Early endosome lumen Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Early endosome lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Postsynaptic early endosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Postsynaptic early endosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Postsynaptic early endosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Postsynaptic early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Extrinsic component of postsynaptic early endosome membrane Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Extrinsic component of postsynaptic early endosome membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Early endosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early endosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Early phagosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early phagosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Early recombination nodule Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early recombination nodule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Early endosome membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early endosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Early endosome lumen Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early endosome lumen cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cytoplasmic side of early endosome membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytoplasmic side of early endosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Early phagosome membrane Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Early phagosome membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Very early onset inflammatory bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Very early onset inflammatory bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive early-onset Parkinson disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive early-onset Parkinson disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early onset and severe retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset and severe retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset coronary artery disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset generalized limb-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset generalized limb-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-childhood-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited polyposis and early onset colorectal cancer - germline testing Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited polyposis and early onset colorectal cancer - germline testing phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early T cell progenitor acute lymphoblastic leukemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early T cell progenitor acute lymphoblastic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Death in early adulthood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in early adulthood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
STAT3-related early-onset multisystem autoimmune disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the STAT3-related early-onset multisystem autoimmune disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset Parkinson disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset Parkinson disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset autosomal dominant Alzheimer disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset autosomal dominant Alzheimer disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early onset focal segmental glomerulosclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early onset focal segmental glomerulosclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early age onset of sporadic thoracic aortic dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset Lafora body disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset Lafora body disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset dementia of unclear Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset dementia of unclear phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset chronic pancreatitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset chronic pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset parkinsonism-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset parkinsonism-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset anterior polar cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset anterior polar cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Anthracycline-induced cardiotoxicity in early breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anthracycline-induced cardiotoxicity in early breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early-onset ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early-onset ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early response to risperidone in schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early response to risperidone in schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early childhood aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early childhood aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Middle childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Kidney disease (early and late stages) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (early and late stages) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early-onset Parkinson's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early-onset Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Estrone conjugates/estrone ratio in resected early stage estrogen-receptor positive breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Estrone conjugates/estrone ratio in resected early stage estrogen-receptor positive breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Estrone/androstenedione ratio in resected early stage-receptor positive breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Estrone/androstenedione ratio in resected early stage-receptor positive breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Plasma androstenedione levels in resected early stage-receptor positive breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma androstenedione levels in resected early stage-receptor positive breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Plasma estrone conjugates levels in resected early stage estrogen-receptor positive breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma estrone conjugates levels in resected early stage estrogen-receptor positive breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Prostate cancer (early onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Prostate cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gemcitabine-induced early high-grade neutropenia in pancreatic cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gemcitabine-induced early high-grade neutropenia in pancreatic cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early diabetic kidney disease in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early diabetic kidney disease in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiopurine-induced early leukopenia in Crohn's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiopurine-induced early leukopenia in Crohn's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proinsulin levels (early-phase conversion) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proinsulin levels (early-phase conversion) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pediatric central nervous system tumors (early onset)(pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric central nervous system tumors (early onset)(pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

epileptic encephalopathy, early infantile, 8 Gene Set

Early infantile epileptic encephalopathy 9 Gene Set

Early infantile epileptic encephalopathy 8 Gene Set

Early infantile epileptic encephalopathy 2 Gene Set

Early infantile epileptic encephalopathy 7 Gene Set

Early infantile epileptic encephalopathy 5 Gene Set

Early infantile epileptic encephalopathy 4 Gene Set

Epileptic encephalopathy, early infantile, 1 Gene Set

Epileptic encephalopathy, early infantile, 23 Gene Set

Early infantile epileptic encephalopathy 18 Gene Set

Early infantile epileptic encephalopathy 13 Gene Set

Early infantile epileptic encephalopathy 10 Gene Set

Early infantile epileptic encephalopathy 17 Gene Set

Early infantile epileptic encephalopathy 16 Gene Set

Early infantile epileptic encephalopathy 14 Gene Set

Early infantile epileptic encephalopathy 11 Gene Set

Epileptic encephalopathy, early infantile, 28 Gene Set

Epileptic encephalopathy, early infantile, 24 Gene Set

Epileptic encephalopathy, early infantile, 25 Gene Set

Epileptic encephalopathy, early infantile, 26 Gene Set

Epileptic encephalopathy, early infantile, 27 Gene Set

Epileptic encephalopathy, early infantile, 21 Gene Set

Epileptic encephalopathy, early infantile, 19 Gene Set

Epileptic Encephalopathy, Early Infantile, 4 Gene Set

Epileptic Encephalopathy, Early Infantile, 1 Gene Set

Epileptic Encephalopathy, Early Infantile, 2 Gene Set

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set

Epileptic Encephalopathy, Early Infantile, 3 Gene Set

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set

epileptic encephalopathy, early infantile, 2 Gene Set

epileptic encephalopathy, early infantile, 24 Gene Set

epileptic encephalopathy, early infantile, 25 Gene Set

epileptic encephalopathy, early infantile, 26 Gene Set

epileptic encephalopathy, early infantile, 27 Gene Set

epileptic encephalopathy, early infantile, 23 Gene Set

epileptic encephalopathy, early infantile, 5 Gene Set

epileptic encephalopathy, early infantile, 4 Gene Set

epileptic encephalopathy, early infantile, 7 Gene Set

epileptic encephalopathy, early infantile, 1 Gene Set

epileptic encephalopathy, early infantile, 3 Gene Set

epileptic encephalopathy, early infantile, 9 Gene Set

epileptic encephalopathy, early infantile, 14 Gene Set

epileptic encephalopathy, early infantile, 17 Gene Set

epileptic encephalopathy, early infantile, 15 Gene Set

epileptic encephalopathy, early infantile, 16 Gene Set

epileptic encephalopathy, early infantile, 11 Gene Set

epileptic encephalopathy, early infantile, 13 Gene Set

epileptic encephalopathy, early infantile, 12 Gene Set

epileptic encephalopathy, early infantile, 19 Gene Set

epileptic encephalopathy, early infantile, 18 Gene Set

?epileptic encephalopathy, early infantile, 21 Gene Set

Early Infantile Epileptic Encephalopathy With Suppression Bursts Gene Set

Early Infantile Epileptic Encephalopathy, Refractory Gene Set

Early infantile epileptic encephalopathy Gene Set

Early Infantile Epileptic Encephalopathy Gene Set

Infantile epileptic dyskinetic encephalopathy Gene Set

epileptic encephalopathy, early infanitle, 1 Gene Set

Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set

Undetermined early-onset epileptic encephalopathy Gene Set

Early onset epileptic encephalopathy Gene Set

Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene Set

SNAP25-related early-onset developmental and epileptic encephalopathy Gene Set

Epileptic encephalopathy, childhood-onset Gene Set

Epileptic encephalopathy, Lennox-Gastaut type Gene Set

epileptic encephalopathy Gene Set

epileptic encephalopathy, childhood-onset Gene Set

Epileptic Encephalopathy Gene Set

Epileptic Encephalopathy Gene Set

Developmental and epileptic encephalopathy Gene Set

Developmental and epileptic encephalopathy 14 Gene Set

Developmental and epileptic encephalopathy 13 Gene Set

Developmental and epileptic encephalopathy 26 Gene Set

Developmental and epileptic encephalopathy 4 Gene Set

Developmental and epileptic encephalopathy 2 Gene Set

Developmental and epileptic encephalopathy 1 Gene Set

Developmental and epileptic encephalopathy 28 Gene Set

Developmental and epileptic encephalopathy Gene Set