seizures, benign familial infantile, 4

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Results for "seizures, benign familial infantile, 4": 1001 gene sets

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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.
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.
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.
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.
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 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.
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.
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.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 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.
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.
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.
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 neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seizures, benign neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Benign neonatal seizures Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neonatal seizures from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign neonatal seizures 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.
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.
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.
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.
benign prostatic hyperplasia and benign prostatic enlargement Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hyperplasia and benign prostatic enlargement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Febrile seizures, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial febrile seizures 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
febrile seizures, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3a Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial febrile seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial febrile seizures 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial febrile seizures 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, familial benign Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, benign familial Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial Benign Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Pemphigus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Adult Familial Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Adult Familial Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hematuria, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Convulsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Mesial Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Retina, Familial Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Retina, Familial Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign familial hematuria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial hematuria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial benign fleck retina Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial benign fleck retina in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, with or without seizures, ARX-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 6 from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Seizures, Febrile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Seizures, Febrile from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.
Alcohol Withdrawal Seizures Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol Withdrawal Seizures from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 1 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 3 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 4 from the curated CTD Gene-Disease Associations dataset.
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 2 from the curated CTD Gene-Disease Associations dataset.
Seizures Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Seizures from the curated CTD Gene-Disease Associations dataset.
epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disease models, animal; fever; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease disease models, animal; fever; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seizures; thrombosis, deep vein; systemic sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease seizures; thrombosis, deep vein; systemic sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, temporal lobe; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; malaria; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; malaria; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, systemic; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol withdrawal seizures; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, post-traumatic; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol withdrawal seizures; alcoholism; disease models, animal; Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; disease models, animal; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seizures, febrile; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease seizures, febrile; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, temporal lobe; sclerosis; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; sclerosis; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angelman syndrome; rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hypoglycemia; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hypoglycemia; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene Set From GAD Gene-Disease Associations genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; epilepsy, post-traumatic; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
confusion; epilepsy, temporal lobe; sclerosis; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease confusion; epilepsy, temporal lobe; sclerosis; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
febrile seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease febrile seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol withdrawal delirium; alcohol withdrawal seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal delirium; alcohol withdrawal seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsies, partial; epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsies, partial; epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; seizures; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; seizures; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol withdrawal seizures; alcoholism; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seizures; thrombosis, deep vein Gene Set From GAD Gene-Disease Associations genes associated with the disease seizures; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seizures Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term seizures in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
focal seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the focal seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hyperkinetic seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hyperkinetic seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal motor seizures Gene Set From GWASdb SNP-Phenotype Associations genes associated with the focal motor seizures phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal seizures with impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures with impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
seizures Gene Set From HPO Gene-Disease Associations genes associated with the seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures without impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
photosensitive tonic-clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the photosensitive tonic-clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the atonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hemiclonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the hemiclonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypocalcemic seizures Gene Set From HPO Gene-Disease Associations genes associated with the hypocalcemic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
developmental stagnation at onset of seizures Gene Set From HPO Gene-Disease Associations genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence seizures Gene Set From HPO Gene-Disease Associations genes associated with the absence seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized myoclonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized myoclonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal motor seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal motor seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic-clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic-clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symptomatic seizures Gene Set From HPO Gene-Disease Associations genes associated with the symptomatic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dialeptic seizures Gene Set From HPO Gene-Disease Associations genes associated with the dialeptic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
febrile seizures Gene Set From HPO Gene-Disease Associations genes associated with the febrile seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral convulsive seizures Gene Set From HPO Gene-Disease Associations genes associated with the bilateral convulsive seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the focal clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoglycemic seizures Gene Set From HPO Gene-Disease Associations genes associated with the hypoglycemic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Seizures, Febrile Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Seizures, Febrile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcohol Withdrawal Seizures Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Withdrawal Seizures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Seizures Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Seizures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
clonic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the clonic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
minimal clonic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the minimal clonic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
environmentally induced seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the environmentally induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
tonic-clonic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the tonic-clonic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sporadic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sporadic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
maximal tonic hindlimb extension seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the maximal tonic hindlimb extension seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
audiogenic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the audiogenic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nonconvulsive seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nonconvulsive seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absence seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absence seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
tonic seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the tonic seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to pharmacologically induced seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
convulsive seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the convulsive seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to pharmacologically induced seizures Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
polymicrogyria with seizures Gene Set From OMIM Gene-Disease Associations genes associated with the polymicrogyria with seizures phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
epilespy, generalized, with febrile seizures plus, type 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epilespy, generalized, with febrile seizures plus, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
?arthrogryposis, mental retardation, and seizures Gene Set From OMIM Gene-Disease Associations genes associated with the ?arthrogryposis, mental retardation, and seizures phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, seizures, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, seizures, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy with febrile seizures plus, type 9 Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
primary aldosteronism, seizures, and neurologic abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the primary aldosteronism, seizures, and neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complex Partial Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complex Partial Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tonic - Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tonic - Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Myoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Post Traumatic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Post Traumatic Seizures 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.
Generialized Epilepsy With Febrile Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generialized Epilepsy With Febrile Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Salaam Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Salaam Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol Withdrawal Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Seizures, Afebril Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Seizures, Afebril in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Myoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Aldosteronism, Seizures, And Neurologic Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Aldosteronism, Seizures, And Neurologic Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Photosensitive Tonic-Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Photosensitive Tonic-Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocalcemic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocalcemic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Tonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Migrating Partial Seizures In Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Migrating Partial Seizures In Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Tonic-Clonic Seizures With Focal Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tonic-Clonic Seizures With Focal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Febrile Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Febrile Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jackknife Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jackknife Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Simple Partial Occipital Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Simple Partial Occipital Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemifacial Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemifacial Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures In The Newborn, Refractory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Seizures In The Newborn, Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uncinate Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uncinate Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Photomyoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Photomyoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperglycinemia, Lactic Acidosis, And Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperglycinemia, Lactic Acidosis, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, 7 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus, 7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atonic Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atonic Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype 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.
Generalized Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Myoclonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonepileptic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonepileptic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Seizures, Auditory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Auditory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Seizures, Focal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Focal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Seizures, Intractable Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Intractable in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Seizures, Sensory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Sensory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Seizures, Somatosensory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Somatosensory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Maternal Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Typical Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Typical Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multifocal Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multifocal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic-Clonic Seizures On Awakening Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic-Clonic Seizures On Awakening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Segmental Myoclonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Segmental Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Stagnation At Onset Of Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Stagnation At Onset Of Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hemiclonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hemiclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nocturnal Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nocturnal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Simple Partial Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Simple Partial Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absence seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absence seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
audiogenic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the audiogenic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to pharmacologically induced seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
tonic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the tonic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
convulsive seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the convulsive seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nonconvulsive seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nonconvulsive seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sporadic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sporadic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to pharmacologically induced seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
tonic-clonic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the tonic-clonic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
maximal tonic hindlimb extension seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the maximal tonic hindlimb extension seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
clonic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the clonic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
environmentally induced seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the environmentally induced seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
minimal clonic seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the minimal clonic seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
febrile seizures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the febrile seizures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
convulsive seizures Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the convulsive seizures phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) pathway from the Reactome Pathways 2024 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized epilepsy with febrile seizures plus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease microcephaly, seizures, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
microcephaly, seizures, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease microcephaly, seizures, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
microcephaly, growth deficiency, seizures, and brain malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease microcephaly, growth deficiency, seizures, and brain malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay and seizures with or without movement abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Seizures-scoliosis-macrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Seizures-scoliosis-macrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Febrile seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Febrile seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pyridoxal phosphate-responsive seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyridoxal phosphate-responsive seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental delay and seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental delay and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome 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.
Intellectual disability and seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNAO1-related developmental delay-seizures-movement disorder spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Malignant migrating partial seizures of infancy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant migrating partial seizures of infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome 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.
Febrile seizures Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Febrile seizures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Febrile seizures (MMR vaccine-unrelated) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Febrile seizures (MMR vaccine-unrelated) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Febrile seizures (MMR vaccine-related) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Febrile seizures (MMR vaccine-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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, 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.
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.
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.
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.
{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.
?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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
Angiotensin i-converting enzyme, benign serum increase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angiotensin i-converting enzyme, benign serum increase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyskeratosis, Hereditary Benign Intraepithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dyskeratosis, Hereditary Benign Intraepithelial from the curated CTD Gene-Disease Associations dataset.
Histiocytoma, Benign Fibrous Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytoma, Benign Fibrous from the curated CTD Gene-Disease Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigoid, Benign Mucous Membrane from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Benign Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Benign Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset.
Benign essential blepharospasm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Benign essential blepharospasm from the curated CTD Gene-Disease Associations dataset.
Benign Paroxysmal Positional Vertigo Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Benign Paroxysmal Positional Vertigo from the curated CTD Gene-Disease Associations dataset.
Vertigo, Benign Recurrent, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertigo, Benign Recurrent, 2 from the curated CTD Gene-Disease Associations dataset.
Telangiectasia, Hereditary Benign Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Benign from the curated CTD Gene-Disease Associations dataset.
integumentary system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease integumentary system benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cell type benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cell type benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease organ system benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease skin benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease organ system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
uterine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease uterine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
female reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
thoracic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign perivascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastrointestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hepatobiliary benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatobiliary benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign essential hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central nervous system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
male reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
musculoskeletal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease musculoskeletal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary tract papillary transitional cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mesenchymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mesenchymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
colonic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colonic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
organ system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease organ system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vaginal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vaginal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
uterine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uterine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urinary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign breast phyllodes tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign breast phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
connective tissue benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease connective tissue benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urethral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urethral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cardiovascular organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign paroxysmal positional nystagmus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign paroxysmal positional nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscle benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscle benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign fibrous mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign fibrous mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gastrointestinal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
kidney benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease kidney benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
integumentary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease integumentary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cell type benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cell type benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign epilepsy with centrotemporal spikes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign epilepsy with centrotemporal spikes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
respiratory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease respiratory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign mammary dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign mammary dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign pleural mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
female reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peritoneal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peritoneal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sensory organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sensory organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
laryngeal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease laryngeal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
immune system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease immune system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duodenal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duodenal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
endocrine organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endocrine organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lung benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bone benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vulvar benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vestibular gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vestibular gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign struma ovarii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign struma ovarii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ureteral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureteral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign peritoneal mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign peritoneal mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign prostatic hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
benign prostatic hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease benign prostatic hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glossitis, benign migratory Gene Set From GAD Gene-Disease Associations genes associated with the disease glossitis, benign migratory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
benign Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term benign in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
gastrointestinal system benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease gastrointestinal system benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
intestinal benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease intestinal benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
organ system benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease organ system benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
uterine benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease uterine benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
female reproductive organ benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
reproductive organ benign neoplasm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
benign neoplasm of the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the benign neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
benign neoplasm of the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the benign neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
benign genitourinary tract neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the benign genitourinary tract neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
benign gastrointestinal tract tumors Gene Set From HPO Gene-Disease Associations genes associated with the benign gastrointestinal tract tumors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Glossitis, Benign Migratory Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glossitis, Benign Migratory phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pemphigoid, Benign Mucous Membrane phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Epilepsy, Benign Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Benign Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
chorea, hereditary benign Gene Set From OMIM Gene-Disease Associations genes associated with the chorea, hereditary benign phenotype from the curated OMIM Gene-Disease Associations dataset.
epidermolysis bullosa, generalized atrophic benign Gene Set From OMIM Gene-Disease Associations genes associated with the epidermolysis bullosa, generalized atrophic benign phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
vertigo, benign recurrent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vertigo, benign recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskeratosis, hereditary benign intraepithelial Gene Set From OMIM Gene-Disease Associations genes associated with the dyskeratosis, hereditary benign intraepithelial phenotype from the curated OMIM Gene-Disease Associations dataset.
[angiotensin i-converting enzyme, benign serum increase] Gene Set From OMIM Gene-Disease Associations genes associated with the [angiotensin i-converting enzyme, benign serum increase] phenotype from the curated OMIM Gene-Disease Associations dataset.
{blepharospasm, primary benign} Gene Set From OMIM Gene-Disease Associations genes associated with the {blepharospasm, primary benign} phenotype from the curated OMIM Gene-Disease Associations dataset.
Benign Teratoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Prostatic Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Prostatic Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meningioma, Benign, No Icd-O Subtype Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meningioma, Benign, No Icd-O Subtype in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Recurrent Intrahepatic Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Chondrogenic Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Chondrogenic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytoma, Benign Fibrous Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytoma, Benign Fibrous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Hereditary Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Hereditary Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Tumor Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Tumor Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Paroxysmal Positional Vertigo Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Paroxysmal Positional Vertigo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Melanocytic Nevus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Melanocytic Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Ovarian Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Ovarian Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Brain, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Brain, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Thyroid Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Thyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cyst Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cyst Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glossitis, Benign Migratory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glossitis, Benign Migratory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Stomach Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leydig Cell Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leydig Cell Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Rolandic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Rolandic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Bladder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Endometrial Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Lung Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Struma Ovarii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Struma Ovarii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pemphigoid, Benign Mucous Membrane Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pemphigoid, Benign Mucous Membrane in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyp Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyp Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mastocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mastocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Dermal Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Dermal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mixed Epithelial And Stromal Tumor Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mixed Epithelial And Stromal Tumor Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Colon Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Sweat Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Sweat Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Large Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Experimental Organism Benign Basalioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Experimental Organism Benign Basalioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Epilepsy, Benign, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Benign Telangiectasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Benign Telangiectasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Hematuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Hematuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multicystic Mesothelioma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multicystic Mesothelioma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Concentric Annular Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Concentric Annular Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neuroendocrine Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synovioma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Synovioma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystinosis, Benign, Nonnephropathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystinosis, Benign, Nonnephropathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastric Ulcer Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastric Ulcer Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphocytic Infiltration Of Jessner Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphocytic Infiltration Of Jessner in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Meninges Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Meninges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Cystic Nephroma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Cystic Nephroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Essential Blepharospasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Essential Blepharospasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Cyst Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Cyst Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Epithelial Tumor Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Vascular Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Vascular Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phosphaturic Mesenchymal Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phosphaturic Mesenchymal Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transitional Cell Papilloma, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transitional Cell Papilloma, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Benign Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Benign Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Mesenchymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Mesenchymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endometrial Polyp Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Polyp Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Endometrial Stromal Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Stromal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy, Nonfamilial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy, Nonfamilial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Focal Epilepsy, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Teratoma Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Teratoma Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Odontogenic Tumor, Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Odontogenic Tumor, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Tumor Of Salivary Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Tumor Of Salivary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Pheochromocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Pheochromocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphoepithelial Lesion Of Lacrimal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphoepithelial Lesion Of Lacrimal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Genitourinary Tract Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Genitourinary Tract Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Experimental Organism Benign Keratoacanthoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Experimental Organism Benign Keratoacanthoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Thyroid Nodule Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Thyroid Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Schwannoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Schwannoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Lymphoproliferative Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphoproliferative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Supratentorial Neoplasms Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Supratentorial Neoplasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Pituitary Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Pituitary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Samaritan Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Samaritan Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neoplasm Of Testis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Angiotensin I-Converting Enzyme, Benign Serum Increase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Angiotensin I-Converting Enzyme, Benign Serum Increase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Blepharospasm, Benign Essential, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blepharospasm, Benign Essential, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fasciculation, Benign Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fasciculation, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Benign Paroxysmal Torticollis Of Infancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Benign Paroxysmal Torticollis Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Benign Prostatic Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Benign Prostatic Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cancer, Benign Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cancer, Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Skin benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Skin benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cell type benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Organ system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Integumentary system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pituitary gland benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Endocrine organ benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Connective tissue benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Connective tissue benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Musculoskeletal system benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Musculoskeletal system benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bone benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bone benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cardiovascular organ benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cardiovascular organ benign neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Organ system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Female reproductive organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Uterine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Uterine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Gastrointestinal system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cell type benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Intestinal benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Small intestine benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Small intestine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Integumentary system benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Skin benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Skin benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Endocrine organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pituitary gland benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign paroxysmal positional vertigo Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign paroxysmal positional vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Organ system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Organ system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cell type benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cell type benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign perivascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uterine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uterine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Female reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Endocrine organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endocrine organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cardiovascular organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cardiovascular organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pituitary gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pituitary gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Musculoskeletal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Musculoskeletal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Integumentary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Integumentary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Skin benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skin benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign ileal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign ileal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastrointestinal system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bone benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Small intestine benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Connective tissue benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Connective tissue benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign vascular tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign vascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Colonic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colonic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Parathyroid gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Parathyroid gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Kidney benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Kidney benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Liver benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Liver benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hepatobiliary benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatobiliary benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Respiratory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Respiratory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Laryngeal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Laryngeal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lung benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lung benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign epilepsy with centrotemporal spikes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign epilepsy with centrotemporal spikes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscle benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscle benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vaginal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vaginal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rectal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rectal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mammary dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mammary dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thoracic benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sweat gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sweat gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign giant cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urinary system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Germ cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Germ cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign teratoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Immune system organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immune system organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Male reproductive organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebrovascular benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebrovascular benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Biliary tract benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Biliary tract benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic nervous system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vulvar benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulvar benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gallbladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gallbladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intraductal breast benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intraductal breast benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign breast phyllodes tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign breast phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urinary tract papillary transitional cell benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urinary tract papillary transitional cell benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sensory organ benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign breast adenomyoepithelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign breast adenomyoepithelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rete ovarii benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rete ovarii benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign peritoneal mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign peritoneal mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Eyelid benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eyelid benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ureteral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ureteral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Urethral benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Urethral benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bladder benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bladder benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal pelvis benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal pelvis benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign essential hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bronchial benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bronchial benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Penile benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Penile benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ampulla of Vater benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ampulla of Vater benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Duodenal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Duodenal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subglottis benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subglottis benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gastrointestinal neuroendocrine benign tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastrointestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple benign circumferential skin creases on limbs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign pleural mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peritoneal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peritoneal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nasal cavity benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nasal cavity benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fallopian tube benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fallopian tube benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Maxillary sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Maxillary sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign mastocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign mastocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Frontal sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Frontal sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Paranasal sinus benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paranasal sinus benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nipple benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nipple benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign renovascular hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cecal benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cecal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vestibular gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vestibular gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bartholin's gland benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bartholin's gland benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cervical benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervical benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign fibrous mesothelioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign fibrous mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign hypertensive renal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign hypertensive renal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign prostatic hyperplasia cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Benign prostatic hyperplasia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign hereditary chorea Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign hereditary chorea phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cancer or benign tumor Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cancer or benign tumor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Neonatal Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Neonatal Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign concentric annular macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign concentric annular macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple benign circumferential skin creases on limbs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple benign circumferential skin creases on limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Rolandic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Rolandic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign cystic nephroma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign cystic nephroma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign childhood epilepsy with centro-temporal spikes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia and lower urinary tract symptoms Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign prostatic hyperplasia and/or lower urinary tract symptoms Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign prostatic hyperplasia and/or lower urinary tract symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Familial Mediterranean fever Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, hyperphosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemic nephropathy, familial juvenile, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cancer of breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial aortopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital arthropathy-brachydactyly, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial visceral amyloidosis, Ostertag type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia familial British Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
familial hyperinsulinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia familial 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

seizures, benign familial infantile, 4 Gene Set

Benign familial neonatal-infantile seizures Gene Set

SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set

seizures, benign familial infantile, 1 Gene Set

seizures, benign familial infantile, 2 Gene Set

seizures, benign familial infantile, 3 Gene Set

Benign familial infantile seizures 3 Gene Set

Benign familial infantile seizures 2 Gene Set

Benign familial infantile seizures 5 Gene Set

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

Benign familial neonatal seizures 1 Gene Set

Benign familial neonatal seizures 2 Gene Set

SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set

SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

Convulsions, Benign Familial Infantile, 4 Gene Set

benign familial infantile epilepsy Gene Set

Benign familial infantile epilepsy Gene Set

Benign familial infantile epilepsy Gene Set

benign neonatal seizures Gene Set

seizures, benign neonatal, 1 Gene Set

seizures, benign neonatal, type 2 Gene Set

Benign neonatal seizures Gene Set

Benign neonatal seizures Gene Set

Benign neonatal seizures Gene Set

Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma Gene Set

Benign Infantile Myoclonic Epilepsy Gene Set

COX deficiency, benign infantile mitochondrial myopathy Gene Set

Benign sporadic infantile epilepsy Gene Set

benign prostatic hyperplasia and benign prostatic enlargement Gene Set

Febrile seizures, familial, 4 Gene Set

Febrile seizures, familial, 11 Gene Set

Febrile seizures, familial, 3b Gene Set

Familial febrile seizures 8 Gene Set

febrile seizures, familial, 9 Gene Set

febrile seizures, familial, 8 Gene Set

febrile seizures, familial, 5 Gene Set

febrile seizures, familial, 4 Gene Set

febrile seizures, familial, 7 Gene Set

febrile seizures, familial, 6 Gene Set

febrile seizures, familial, 1 Gene Set

febrile seizures, familial, 2 Gene Set

febrile seizures, familial, 11 Gene Set

febrile seizures, familial, 10 Gene Set

febrile seizures, familial, 3a Gene Set

febrile seizures, familial, 3b Gene Set

Familial febrile seizures Gene Set

Familial febrile seizures 11 Gene Set

Familial febrile seizures 2 Gene Set

Familial febrile seizures 4 Gene Set

Familial febrile seizures 6 Gene Set

Familial febrile seizures 5 Gene Set

Familial febrile seizures 1 Gene Set

Familial febrile seizures 9 Gene Set

Familial febrile seizures 7 Gene Set

Familial febrile seizures 10 Gene Set

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

Familial infantile myasthenia Gene Set

Myoclonic epilepsy, familial infantile Gene Set

Myasthenia, Familial Infantile, 1 Gene Set

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

myasthenia, familial infantile, 1 Gene Set

myoclonic epilepsy, infantile, familial Gene Set

convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set

Familial Infantile Myasthenia Gene Set

Myasthenia, Familial Infantile, 1 Gene Set

Infantile Convulsions And Paroxysmal Choreoathetosis, Familial (Disorder) Gene Set

Familial infantile myasthenia Gene Set

Self-limited familial infantile epilepsy Gene Set

Familial infantile myoclonic epilepsy Gene Set

Episodic kinesigenic dyskinesia and familial infantile convulsions Gene Set

Familial infantile bilateral striatal necrosis Gene Set

Thrombocytosis, benign familial microcytic Gene Set

Familial benign pemphigus Gene Set

Familial benign hypercalcemia Gene Set

Benign familial hematuria Gene Set

Fleck retina, familial benign Gene Set

Pemphigus, Benign Familial Gene Set

Hematuria, Benign Familial Gene Set

Familial benign hypercalcemia, type 3 Gene Set